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Name:Aminosyn Ii With Electrolytes
Manufacturer:Hospira, Inc.
Category:Prescription Marketed Drugs


Aminosyn® II 8.5% WITH ELECTROLYTESSulfite-Free

AMINOSYN II WITH ELECTROLYTES - isoleucine, leucine, lysine acetate, methionine, phenylalanine, threonine, tryptophan, alanine, arginine, histidine, proline, serine, glycine, valine, aspartic acid, n-acetyl-tyrosine, glutamic acid, magnesium chloride, sodium phosphate, dibasic, sodium chloride and potassium chloride injection, solution 
Hospira, Inc.

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Aminosyn® II 8.5% WITH ELECTROLYTES
Sulfite-Free

AN AMINO ACID INJECTION WITH ELECTROLYTES

Flexible Plastic Container

Rx only

DESCRIPTION

Aminosyn® II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection with electrolytes) is a sterile, nonpyrogenic solution for intravenous infusion. Aminosyn II 8.5% WITH ELECTROLYTES is oxygen sensitive. The following formulation is available:

Essential Amino Acids (mg/100 mL)

Isoleucine

561

Leucine

850

Lysine (acetate)*

893

Methionine

146

Phenylalanine

253

Threonine

340

Tryptophan

170

Valine

425

* Amount cited is for lysine alone and does not include the acetate salt.


Nonessential Amino Acids (mg/100 mL)

Alanine

844

Arginine

865

L-Aspartic Acid

595

L-Glutamic Acid

627

Histidine

255

Proline

614

Serine

450

N-Acetyl-L-Tyrosine

230

Glycine

425


Product Characteristics

Protein Equivalent (approx. g/liter)

85

Total Nitrogen (g/liter)

13.0

Osmolarity (mOsmol/L)

920

pHa

5.8

range

5.0 - 6.5

a Contains sodium hydroxide for pH adjustment.


Electrolytes (mEq/liter)

Sodium (Na+)b

78

Potassium (K+)

66

Magnesium (Mg++)

10

Phosphorus mMc

30

Chloride (Cl¯)

86

Acetate (C2H3O2‾)

61d

b Includes sodium from the pH adjustor.

c mM = millimoles; one mM of phosphorus = 31 mg P.

d Includes acetate from lysine acetate.


Electrolytes (mg/100 mL)

Sodium Chloridee

60 mg

Magnesium Chloride hexahydratef

102 mg

Sodium Phosphate, dibasicg

425 mg

Potassium Chlorideh

492 mg

e Sodium Chloride, USP is chemically designated NaCl, a white crystalline powder freely soluble in water.

f Magnesium Chloride, USP is chemically designated magnesium chloride, hexahydrate, MgCl2 • 6H2O, deliquescent crystals very soluble in water.

g Sodium Phosphate, dibasic, USP is chemically designated Na2HPO4, white granules very soluble in water.

h Potassium Chloride, USP is chemically designated KCl, a white granular powder freely soluble in water.

The formulas for the individual amino acids present in Aminosyn II 8.5% WITH ELECTROLYTES are as follows:

Essential Amino Acids

Isoleucine, USP

C6H13NO2

Leucine, USP

C6H13NO2

Lysine Acetate, USP

C6H14N2O2 • CH3COOH

Methionine, USP

C5H11NO2S

Phenylalanine, USP

C9H11NO2

Threonine, USP

C4H9NO3

Tryptophan, USP

C11H12N2O2

Valine, USP

C5H11NO2

Nonessential Amino Acids

Alanine, USP

C3H7NO2

Arginine, USP

C6H14N4O2

L-Aspartic Acid

C4H7NO4


HO2CCH2CH(NH2)CO2H

L-Glutamic Acid

C5H9NO4


HO2CCH2CH2CH(NH2)CO2H

Glycine, USP

C2H5NO2

Histidine, USP

C6H9N3O2

Proline, USP

C5H9NO2

Serine, USP

C3H7NO3

N-Acetyl-L-Tyrosine

C11H13NO4

structural formula N-Acetyl-L-Tyrosine

The flexible plastic container is fabricated from a specially formulated polyvinylchloride. Water can permeate from inside the container into the overwrap but not in amounts sufficient to affect the solution significantly.

Solutions in contact with the plastic container may leach out certain chemical components from the plastic in very small amounts; however, biological testing was supportive of the safety of the plastic container materials.

Exposure to temperatures above 25°C/77°F during transport and storage will lead to minor losses in moisture content. Higher temperatures lead to greater losses. It is unlikely that these minor losses will lead to clinically significant changes within the expiration period.

CLINICAL PHARMACOLOGY

Aminosyn II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection with electrolytes) provides crystalline amino acids to promote protein synthesis and wound healing, and to reduce the rate of endogenous protein catabolism. Aminosyn II 8.5% WITH ELECTROLYTES, given by central venous infusion in combination with concentrated dextrose, electrolytes, vitamins, trace metals, and ancillary fat supplements, constitutes total parenteral nutrition (TPN). Aminosyn II 8.5% WITH ELECTROLYTES can also be administered by peripheral vein with dextrose and maintenance electrolytes. Intravenous fat emulsion may be substituted for part of the carbohydrate calories during either TPN or peripheral vein administration of Aminosyn II 8.5% WITH ELECTROLYTES.

INDICATIONS AND USAGE

Aminosyn II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection) infused with dextrose by peripheral vein infusion is indicated as a source of nitrogen in the nutritional support of patients in whom, for short periods of time, oral nutrition cannot be tolerated, is undesirable, or inadequate.

Aminosyn II 8.5% WITH ELECTROLYTES can be administered peripherally with dilute (5 to 10%) dextrose solution and I.V. fat emulsion as a source of nutritional support. This form of nutritional support can help to preserve protein and reduce catabolism in stress conditions where oral intake is inadequate.

When administered with concentrated dextrose solution with or without fat emulsions, Aminosyn II 8.5% WITH ELECTROLYTES is also indicated for central vein infusion to prevent or reverse negative nitrogen balance in patients where: (a) the alimentary tract, by the oral, gastrostomy or jejunostomy route cannot or should not be used; (b) gastrointestinal absorption of protein is impaired; (c) metabolic requirements for protein are substantially increased as with extensive burns and (d) morbidity and mortality may be reduced by replacing amino acids lost from tissue breakdown, thereby preserving tissue reserves, as in acute renal failure.

CONTRAINDICATIONS

This preparation should not be used in patients with hepatic coma or metabolic disorders involving impaired nitrogen utilization.

WARNINGS

Intravenous infusion of amino acids may induce a rise in blood urea nitrogen (BUN), especially in patients with impaired hepatic or renal function. Appropriate laboratory tests should be performed periodically and infusion discontinued if BUN levels exceed normal postprandial limits and continue to rise. It should be noted that a modest rise in BUN normally occurs as a result of increased protein intake.

Administration of amino acid solutions to a patient with hepatic insufficiency may result in serum amino acid imbalances, metabolic alkalosis, prerenal azotemia, hyperammonemia, stupor and coma.

Administration of amino acid solutions in the presence of impaired renal function may augment an increasing BUN, as does any protein dietary component.

Solutions containing sodium ion should be used with great care, if at all, in patients with congestive heart failure, severe renal insufficiency and in clinical states in which there exists edema with sodium retention.

Solutions which contain potassium ion should be used with great care, if at all, in patients with hyperkalemia, severe renal failure and in conditions in which potassium retention is present.

Solutions containing acetate ion should be used with great care in patients with metabolic or respiratory alkalosis. Acetate should be administered with great care in those conditions in which there is an increased level or an impaired utilization of this ion, such as severe hepatic insufficiency.

Aminosyn II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection) may not be suitable for use in infants who require individualized electrolyte therapy.

Hyperammonemia is of special significance in infants, as it can result in mental retardation. Therefore, it is essential that blood ammonia levels be measured frequently in infants.

Instances of asymptomatic hyperammonemia have been reported in patients without overt liver dysfunction. The mechanisms of this reaction are not clearly defined, but may involve genetic defects and immature or subclinically impaired liver function.

WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.

Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.

PRECAUTIONS

Special care must be taken when administering glucose to provide calories in diabetic or prediabetic patients.

Feeding regimens which include amino acids should be used with caution in patients with history of renal disease, pulmonary disease, or with cardiac insufficiency so as to avoid excessive fluid accumulation.

The effect of infusion of amino acids, without dextrose, upon carbohydrate metabolism of children is not known at this time.

Nitrogen intake should be carefully monitored in patients with impaired renal function.

For long-term total nutrition, or if a patient has inadequate fat stores, it is essential to provide adequate exogenous calories concurrently with the amino acids. Concentrated dextrose solutions are an effective source of such calories. Such strongly hypertonic nutrient solutions should be administered through an indwelling intravenous catheter with the tip located in the superior vena cava.

SPECIAL PRECAUTIONS FOR CENTRAL VENOUS INFUSIONS

ADMINISTRATION BY CENTRAL VENOUS CATHETER SHOULD BE USED ONLY BY THOSE FAMILIAR WITH THIS TECHNIQUE AND ITS COMPLICATIONS.

Central vein infusion (with added concentrated carbohydrate solutions) of amino acid solutions requires a knowledge of nutrition as well as clinical expertise in recognition and treatment of complications. Attention must be given to solution preparation, administration and patient monitoring. IT IS ESSENTIAL THAT A CAREFULLY PREPARED PROTOCOL BASED ON CURRENT MEDICAL PRACTICES BE FOLLOWED, PREFERABLY BY AN EXPERIENCED TEAM.

SUMMARY HIGHLIGHTS OF COMPLICATIONS (consult current medical literature).

  1. Technical

    The placement of a central venous catheter should be regarded as a surgical procedure. One  should be fully acquainted with various techniques of catheter insertion. For details of technique  and placement sites, consult the medical literature. X-ray is the best means of verifying catheter  placement. Complications known to occur from the placement of central venous catheters are  pneumothorax, hemothorax, hydrothorax, artery puncture and transection, injury to the brachial plexus, malposition of the catheter, formation of arteriovenous fistula, phlebitis, thrombosis and  air and catheter emboli.

  2. Septic

    The constant risk of sepsis is present during administration of total parenteral nutrition. It is  imperative that the preparation of the solution and the placement and care of catheters be  accomplished under strict aseptic conditions.

    Solutions should ideally be prepared in the hospital pharmacy under a laminar flow hood using  careful aseptic technique to avoid inadvertent touch contamination. Solutions should be used promptly after mixing. Storage should be under refrigeration and limited to a brief period of  time, preferably less than 24 hours.

    Administration time for a single container and set should never exceed 24 hours.

  3. Metabolic

    The following metabolic complications have been reported with TPN administration: metabolic  acidosis and alkalosis, hypophosphatemia, hypocalcemia, osteoporosis, hyperglycemia,  hyperosmolar nonketotic states and dehydration, glycosuria, rebound hypoglycemia, osmotic  diuresis and dehydration, elevated liver enzymes, hypo- and hypervitaminosis, electrolyte  imbalances and hyperammonemia in children. Frequent evaluations are necessary especially  during the first few days of therapy to prevent or minimize these complications.

    Administration of glucose at a rate exceeding the patient’s utilization rate may lead to  hyperglycemia, coma and death.

Pregnancy Category C

Animal reproduction studies have not been conducted with Aminosyn II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection). It is not known whether Aminosyn II 8.5% WITH ELECTROLYTES can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Aminosyn II 8.5% WITH ELECTROLYTES should be given to a pregnant woman only if clearly needed.

Geriatric Use

Clinical studies of Aminosyn II 8.5% WITH ELECTROLYTES have not been performed to determine whether patients over 65 years respond differently from younger subjects. Other reported clinical experience has not identified differences in responses between elderly and younger patients. In general, dose selection for elderly patients should be cautious, reflecting the greater frequency of decreased hepatic, renal, or cardiac function, and of concomitant disease or other drug therapy. This drug is known to be substantially excreted by the kidney, and the risk of toxic reactions to this drug may be greater in patients with impaired renal function. Because elderly patients are more likely to have decreased renal function, care should be taken in dose selection, and it may be useful to monitor renal functions.

CLINICAL EVALUATION AND LABORATORY DETERMINATIONS, AT THE DISCRETION OF THE ATTENDING PHYSICIAN, ARE NECESSARY FOR PROPER MONITORING DURING ADMINISTRATION. Do not withdraw venous blood for blood chemistries through the peripheral infusion site, as interference with estimations of nitrogen containing substances may occur. Blood studies should include glucose, urea nitrogen, serum electrolytes, ammonia, cholesterol, acid-base balance, serum proteins, kidney and liver function tests, osmolarity and hemogram. White blood count and blood cultures are to be determined if indicated. Urinary osmolality and glucose should be determined as necessary.

Aminosyn II 8.5% WITH ELECTROLYTES contains no more than 25 mcg/L of aluminum.

Drug Interactions

Because of its antianabolic activity, concurrent administration of tetracycline may reduce the potential anabolic effects of amino acids infused with dextrose as part of a parenteral feeding regimen.

Additives may be incompatible. Consult with pharmacist if available. When introducing additives, use aseptic technique, mix thoroughly and do not store.

ADVERSE REACTIONS

Peripheral Infusions

A 3.5% to 5% solution of amino acids (without additives) is slightly hypertonic. Local reactions consisting of a warm sensation, erythema, phlebitis and thrombosis at the infusion site have occurred with peripheral intravenous infusion of amino acids particularly if other substances, such as antibiotics, are also administered through the same site. In such cases the infusion site should be changed promptly to another vein. Use of large peripheral veins, inline filters, and slowing the rate of infusion may reduce the incidence of local venous irritation. Electrolyte additives should be spread throughout the day. Irritating additive medications may need to be infused at another venous site.

Generalized flushing, fever and nausea also have been reported during peripheral infusions of amino acid solutions.

OVERDOSAGE

In the event of overhydration or solute overload, re-evaluate the patient and institute appropriate corrective measures. See WARNINGS and PRECAUTIONS.

DOSAGE AND ADMINISTRATION

The total daily dose of the solution depends on the daily protein requirements and on the patient’s metabolic and clinical response. In many patients, provision of adequate calories in the form of hypertonic dextrose may require the administration of exogenous insulin to prevent hyperglycemia and glycosuria. To prevent rebound hypoglycemia, a solution containing 5% dextrose should be administered when hypertonic dextrose infusions are abruptly discontinued.

Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit. COLOR VARIATION FROM PALE YELLOW TO YELLOW IS NORMAL AND DOES NOT ALTER EFFICACY.

Central Vein Total Parenteral Nutrition

For central vein infusion with concentrated dextrose solution, alone or with I.V. lipid, the total daily dose of the amino acid solution depends upon daily protein requirements and the patient’s metabolic and clinical response. The determination of nitrogen balance and accurate daily body weights, corrected for fluid balance, are probably the best means of assessing individual protein requirements.

Adults

Admixtures of 3.5 to 4.25% amino acids with 5 to 10% dextrose may be infused with a fat emulsion by peripheral vein to provide approximately 1400 to 2000 kcal/day. Fat emulsion administration should be considered when prolonged parenteral nutrition is required in order to prevent essential fatty acid deficiency (E.F.A.D.). Serum lipids should be monitored for evidence of E.F.A.D. in patients maintained on fat-free TPN.

Aminosyn II 8.5% WITH ELECTROLYTES, Sulfite-Free, (an amino acid injection) should only be infused via a central vein when admixed with sufficient dextrose to provide full caloric requirements in patients who require prolonged total parenteral nutrition. I.V. lipid may be administered to provide part of the calories, if desired. Serum lipids should be monitored for evidence of essential fatty acid deficiency in patients maintained on fat-free TPN.

Total parenteral nutrition (TPN) may be started with 10% dextrose added to the calculated daily requirement of amino acids (1.5 g/kg for a metabolically stable patient). Dextrose content is gradually increased over the next few days to the estimated daily caloric need as the patient adapts to the increasing amounts of dextrose. Each gram of dextrose provides approximately 3.4 kcal. Each gram of fat provides 9 kcal.

The average depleted major surgical patient with complications requires between 2500 and 4000 kcal and between 12 and 24 grams of nitrogen per day. An adult patient in an acceptable weight range with restricted activity who is not hypermetabolic, requires about 30 kcal/kg of body weight/day. Average daily adult fluid requirements are between 2500 and 3000 mL and may be much higher with losses from fistula drainage or in severe burns. Typically, a hospitalized patient may lose 12 to 18 grams of nitrogen a day, and in severe trauma the daily loss may be 20 to 25 grams or more.

Aminosyn II 8.5% WITH ELECTROLYTES is designed to supply necessary electrolytes to patients in a stable metabolic state (about three-fourths of all patients on total parenteral nutrition). Other patients may require more or less of the electrolytes present, e.g., cardiac patients who should not receive sodium. Aminosyn II 8.5% WITH ELECTROLYTES does not contain calcium, and this should be added as indicated.

SERUM ELECTROLYTES SHOULD BE MONITORED AS INDICATED. Electrolytes may be added to the nutrient solution as indicated by the patient’s clinical condition and laboratory determinations of plasma values. Major electrolytes are sodium, chloride, potassium, phosphate, magnesium and calcium. Vitamins, including folic acid and vitamin K are required additives. The trace element supplements should be given when long-term parenteral nutrition is undertaken.

Calcium and phosphorus are added to the solution as indicated. The usual dose of phosphorus added to a liter of TPN solution (containing 25% dextrose) is 12 mM. This requirement is related to the carbohydrate calories delivered. Iron is added to the solution or given intramuscularly in depot form as indicated. Vitamin B12, vitamin K and folic acid are given intramuscularly or added to the solution as desired.

Calcium and phosphorus additives are potentially incompatible when added to the TPN admixture. However, if one additive is added to the amino acid container, and the other to the container of concentrated dextrose, and if the contents of both containers are swirled before they are combined, then the likelihood of physical incompatibility is reduced.

In patients with hyperchloremic or other metabolic acidosis, sodium and potassium may be added as the acetate or lactate salts to provide bicarbonate alternates.

In adults, hypertonic mixtures of amino acids and dextrose may be safely administered by continuous infusion through a central venous catheter with the tip located in the vena cava. Typically, the 8.5% solution is used in equal volume with 50% or 70% dextrose to provide an admixture containing 4.25% amino acids and 25% or 35% dextrose respectively.

The rate of intravenous infusion initially should be 2 mL/min and may be increased gradually. If administration should fall behind schedule, no attempt to “catch up” to planned intake should be made. In addition to meeting protein needs, the rate of administration is governed by the patient’s glucose tolerance estimated by glucose levels in blood and urine.

Aminosyn II 8.5% WITH ELECTROLYTES solution, when mixed with an appropriate volume of concentrated dextrose, offers a higher concentration of calories and nitrogen per unit volume. This solution is indicated for patients requiring larger amounts of nitrogen than could otherwise be provided or where total fluid load must be kept to a minimum, for example, patients with renal failure.

Provision of adequate calories in the form of hypertonic dextrose may require exogenous insulin to prevent hyperglycemia and glycosuria. To prevent rebound hypoglycemia, do not abruptly discontinue administration of nutritional solutions.

Pediatric

Aminosyn II 8.5% WITH ELECTROLYTES may not be suitable for use in infants whose electrolyte requirements must be “custom tailored” based on serial blood chemistry determinations.

Pediatric requirements for parenteral nutrition are constrained by the greater relative fluid requirements of the infant and greater caloric requirements per kilogram. Amino acids are probably best administered in a 2.5% concentration. For most pediatric patients on intravenous nutrition, 2.5 grams amino acids/kg/day with dextrose alone or with I.V. lipid calories of 100 to 130 kcal/kg/day is recommended. In cases of malnutrition or stress, these requirements may be increased. It is acceptable in pediatrics to start with a nutritional solution of half strength at a rate of about 60 to 70 mL/kg/day. Within 24 to 48 hours the volume and concentration of the solution can be increased until the full strength pediatric solution (amino acids and dextrose) is given at a rate of 125 to 150 mL/kg/day.

Supplemental electrolytes and vitamin additives should be administered as deemed necessary by careful monitoring of blood chemistries and nutritional status. Addition of iron is more critical in the infant than the adult because of the increasing red cell mass required for the growing infant. Serum lipids should be monitored for evidence of essential fatty acid deficiency in patients maintained on fat-free TPN. Bicarbonate should not be administered during infusion of the nutritional solution unless deemed absolutely necessary.

To ensure the precise delivery of the small volumes of fluid necessary for total parenteral nutrition in infants, accurately calibrated and reliable infusion systems should be used.

A basic solution for pediatric use should contain 25 grams of amino acids and 200 to 250 grams of glucose per 1000 mL, administered from containers containing 250 or 500 mL. Such a solution given at the rate of 145 mL/kg/day provides 130 kcal/kg/day.

WARNING: Do not use flexible container in series connections.

HOW SUPPLIED

NDC No.

Concentration

Container (mL)

0409-4171-03

Aminosyn II 8.5% WITH ELECTROLYTES,

Sulfite-Free, (an amino acid injection)

500

Store at 20 to 25°C (68 to 77°F). [See USP Controlled Room Temperature.] Protect from freezing. Avoid exposure to light.

Revised: August, 2008

Printed in USA

EN-1771

Hospira, Inc., Lake Forest, IL 60045 USA


IM-0755

bag ndc 0409-4171-03

WR-0282

overwrap ndc 0409-4171-03


AMINOSYN II WITH ELECTROLYTES 
isoleucine,leucine,lysine acetate,methionine,phenylalanine,threonine,tryptophan,alanine,arginine,histidine,proline,serine,glycine,valine,aspartic acid,n-acetyl-tyrosine,glutamic acid,magnesium chloride,sodium phosphate, dibasic,sodium chloride,potassium chloride injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:0409-4171
Route of Administration INTRAVENOUS DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Isoleucine (Isoleucine) Isoleucine 561 mg  in 100 mL
Leucine (Leucine) Leucine 850 mg  in 100 mL
LYSINE ACETATE (Lysine) Lysine 893 mg  in 100 mL
Methionine (Methionine) Methionine 146 mg  in 100 mL
Phenylalanine (Phenylalanine) Phenylalanine 253 mg  in 100 mL
Threonine (Threonine) Threonine 340 mg  in 100 mL
Tryptophan (Tryptophan) Tryptophan 170 mg  in 100 mL
Alanine (Alanine) Alanine 844 mg  in 100 mL
Arginine (Arginine) Arginine 865 mg  in 100 mL
Histidine (Histidine) Histidine 255 mg  in 100 mL
Proline (Proline) Proline 614 mg  in 100 mL
Serine (Serine) Serine 450 mg  in 100 mL
Glycine (Glycine) Glycine 425 mg  in 100 mL
Valine (Valine) Valine 425 mg  in 100 mL
ASPARTIC ACID (ASPARTIC ACID) ASPARTIC ACID 595 mg  in 100 mL
N-ACETYL-TYROSINE (TYROSINE) N-ACETYL-TYROSINE 230 mg  in 100 mL
GLUTAMIC ACID (GLUTAMIC ACID) GLUTAMIC ACID 627 mg  in 100 mL
MAGNESIUM CHLORIDE (MAGNESIUM and CHLORIDE ION) MAGNESIUM CHLORIDE 102 mg  in 100 mL
SODIUM PHOSPHATE, DIBASIC (SODIUM CATION and PHOSPHORUS) SODIUM PHOSPHATE, DIBASIC 425 mg  in 100 mL
SODIUM CHLORIDE (SODIUM CATION and CHLORIDE ION) SODIUM CHLORIDE 60 mg  in 100 mL
POTASSIUM CHLORIDE (POTASSIUM CATION and CHLORIDE ION) POTASSIUM CHLORIDE 492 mg  in 100 mL
Inactive Ingredients
Ingredient Name Strength
Sodium Hydroxide  
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:0409-4171-03 12 BAG (12 BAG) in 1 CASE contains a BAG
1 500 mL in 1 BAG This package is contained within the CASE (0409-4171-03)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
NDA NDA019437 12/24/2009

Labeler - Hospira, Inc. (141588017)

Revised: 12/2009 Hospira, Inc.



Source: http://dailymed.nlm.nih.gov
Reproduced with permission of U.S. National Library of Medicine


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