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Name:Meclizine Hydrochloride
Manufacturer:Udl Laboratories, Inc.
Category:Prescription Marketed Drugs


MECLIZINE HYDROCHLORIDE - meclizine hydrochloride tablet 
UDL Laboratories, Inc.

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DESCRIPTION

Meclizine hydrochloride, an oral antiemetic, is a white, slightly yellowish, crystalline powder which has a slight odor and is tasteless. It has the following structural formula:

chemical structure

C25H27CIN2•2HCI•H2O M.W. 481.89

The chemical name is 1-(p-chloro-alpha-phenylbenzyl)-4-(m-methyl-benzyl) - piperazine dihydrochloride monohydrate.

Meclizine Hydrochloride Tablets are available in 12.5 mg, and *25 mg strengths for oral administration.

*Contains FD&C Yellow #5 (see PRECAUTIONS).

Each tablet contains the following inactive ingredients: colloidal silicon dioxide, lactose, magnesium stearate, microcrystalline cellulose, sodium starch glycolate, starch, and stearic acid. In addition, the 12.5 mg tablet contains FD&C Blue #1; and the 25 mg tablet contains D&C Yellow #10 and FD&C Yellow #5.

CLINICAL PHARMACOLOGY

Meclizine hydrochloride is an antihistamine which shows marked protective activity against nebulized histamine and lethal doses of intravenously injected histamine in guinea pigs. It has a marked effect in blocking the vasodepressor response to histamine, but only a slight blocking action against acetylcholine. Its activity is relatively weak in inhibiting the spasmogenic action of histamine on isolated guinea pig ileum.

INDICATIONS AND USAGE

For the prevention and treatment of nausea, vomiting, or dizziness associated with motion sickness.

CONTRAINDICATIONS

Meclizine hydrochloride is contraindicated in individuals who have shown a previous hypersensitivity to it.

WARNINGS

Since drowsiness may, on occasion, occur with use of this drug, patients should be warned of this possibility and cautioned against driving a car or operating dangerous machinery.

Patients should avoid alcoholic beverages while taking the drug. Due to its potential anticholinergic action, this drug should be used with caution in patients with asthma, glaucoma, or enlargement of the prostate gland. Do not give to children under 12 years of age unless directed by a doctor.

PRECAUTIONS

The Meclizine Hydrochloride Tablets, 25 mg contain FD&C Yellow #5 (tartrazine) which may cause allergic-type reactions (including bronchial asthma) in certain susceptible individuals. Although the overall incidence of FD&C Yellow #5 (tartrazine) sensitivity in the general population is low, it is frequently seen in patients who also have aspirin hypersensitivity.

Usage in Children: Clinical studies establishing safety and effectiveness in children have not been done; therefore, usage is not recommended under 12 years of age.

Usage in Pregnancy:Pregnancy Category B. Reproduction studies in rats have shown cleft palates at 25-50 times the human dose. Epidemiological studies in pregnant women, however, do not indicate that meclizine hydrochloride increases the risk of abnormalities when administered during pregnancy.

Despite the animal findings, it would appear that the possibility of fetal harm is remote. Nevertheless, meclizine hydrochloride, or any other medication should be used during pregnancy only if clearly necessary.

ADVERSE REACTIONS

Drowsiness, dry mouth, and on rare occasions, blurred vision have been reported.

DOSAGE AND ADMINISTRATION

Motion Sickness: The initial dose of 25 to 50 mg meclizine hydrochloride, should be taken one hour prior to travel for protection against motion sickness. Thereafter, the dose may be repeated every 24 hours for the duration of the journey.

HOW SUPPLIED:

Meclizine Hydrochloride Tablets, USP 12.5 mg - blue, oval tablets debossed with “034” on one side and “par” on the other side. Tablets may contain characteristic dye spots. They are available as follows:

NDC 51079-089-20 - Unit dose blister packages of 100 (10 cards of 10 tablets each).

Meclizine Hydrochloride Tablets, USP 25 mg - yellow, oval tablets debossed with “035” on one side and “par” on the other side. They are available as follows:

NDC 51079-090-20 - Unit dose blister packages of 100 (10 cards of 10 tablets each).

Store at controlled room temperature 15° to 30°C (59° to 86°F).

Manufactured by:
Par Pharmaceutical Companies, Inc.
Spring Valley, NY 10977

Distributed by:
UDL Laboratories, Inc.
Rockford, IL 61103

S-5278 R13
3/10

PRINCIPAL DISPLAY PANEL - 12.5 mg

NDC 51079-089-20

MECLIZINE HYDROCHLORIDE
TABLETS, USP
12.5 mg

100 Tablets (10 x 10)

Each tablet contains:
Meclizine HCl, USP . . . . . . 12.5 mg

USUAL DOSAGE: Read Accompanying Literature.

Store at controlled room temperature 15° to 30°C (59° to 86°F).

Manufactured by:
Par Pharmaceutical Companies, Inc.
Spring Valley, NY 10977

Rx only

S-5276 R7

Packaged and Distributed by:

UDL LABORATORIES, INC.

ROCKFORD, IL 61103

This unit dose package is not child resistant.

For institutional use only.

Keep this and all drugs out of the reach of children.

This container provides light-resistance.

See window for lot number and expiration date.

Meclizine Hydrochloride 12.5 mg Tablets
Unit Carton

PRINCIPAL DISPLAY PANEL - 25 mg

NDC 51079-090-20

MECLIZINE HYDROCHLORIDE
TABLETS, USP
25 mg

100 Tablets (10 x 10)

Each tablet contains:
Meclizine HCl, USP . . . . . . 25 mg

USUAL DOSAGE: Read Accompanying Literature.

CAUTION: This product contains FD&C Yellow
No. 5 (tartrazine) which may cause allergic type
reactions in certain susceptible individuals.

Store at controlled room temperature 15° to 30°C (59° to 86°F).

Manufactured by:
Par Pharmaceutical Companies, Inc.
Spring Valley, NY 10977

Rx only

S-5277 R7

Packaged and Distributed by:

UDL LABORATORIES, INC.

ROCKFORD, IL 61103

This unit dose package is not child resistant.

For institutional use only.

Keep this and all drugs out of the reach of children.

This container provides light-resistance.

See window for lot number and expiration date.

Meclizine Hydrochloride 25 mg Tablets
Unit Carton

MECLIZINE HYDROCHLORIDE 
meclizine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51079-090
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 25 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE  
CELLULOSE, MICROCRYSTALLINE  
SODIUM STARCH GLYCOLATE TYPE A POTATO  
STARCH, CORN  
STEARIC ACID  
WATER  
ISOPROPYL ALCOHOL  
D&C YELLOW NO. 10  
MAGNESIUM STEARATE  
COLLOIDAL SILICON DIOXIDE  
Product Characteristics
Color YELLOW Score no score
Shape OVAL Size 6mm
Flavor Imprint Code Par;035
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51079-090-20 100 BLISTER PACK ( BLISTER PACK) in 1 BOX, UNIT-DOSE contains a BLISTER PACK (51079-090-01)
1 NDC:51079-090-01 1 TABLET ( TABLET) in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (51079-090-20)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087128 05/13/2011

MECLIZINE HYDROCHLORIDE 
meclizine hydrochloride tablet
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51079-089
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MECLIZINE HYDROCHLORIDE (MECLIZINE) MECLIZINE HYDROCHLORIDE 12.5 mg
Inactive Ingredients
Ingredient Name Strength
ANHYDROUS LACTOSE  
CELLULOSE, MICROCRYSTALLINE  
SODIUM STARCH GLYCOLATE TYPE A POTATO  
FD&C BLUE NO. 1  
WATER  
ISOPROPYL ALCOHOL  
STARCH, CORN  
STEARIC ACID  
MAGNESIUM STEARATE  
COLLOIDAL SILICON DIOXIDE  
Product Characteristics
Color BLUE Score no score
Shape OVAL Size 5mm
Flavor Imprint Code Par;034
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:51079-089-20 100 BLISTER PACK ( BLISTER PACK) in 1 BOX, UNIT-DOSE contains a BLISTER PACK (51079-089-01)
1 NDC:51079-089-01 1 TABLET ( TABLET) in 1 BLISTER PACK This package is contained within the BOX, UNIT-DOSE (51079-089-20)

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA087127 05/13/2011

Labeler - UDL Laboratories, Inc. (039615992)
Registrant - UDL Laboratories, Inc. (039615992)
Establishment
Name Address ID/FEI Operations
Par Pharmaceutical, Inc. 092733690 MANUFACTURE
Establishment
Name Address ID/FEI Operations
UDL Laboratories, Inc. 039615992 REPACK, RELABEL

Revised: 03/2010 UDL Laboratories, Inc.



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


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