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Name:Nicotine Polacrilex
Manufacturer:Nicobrand Ltd
Category:Prescription Marketed Drugs


Nicotine Polacrilex

NICOTINE POLACRILEX - nicotine powder 
Nicobrand LTD

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Nicotine Polacrilex

PRINCIPAL DISPLAY PANEL – BULK PRODUCT

NAME: Nicotine compound, solid, n.o.s.
      (Nicotine Polacrilex 18%)

NDC Number: 61252-3002-<>

UN No.: UN 1655

CAUTION:
for manufacturing,
processing or repacking.

Manufactured by: Nicobrand Limited
189 Castleroe Road, Coleraine
N. Ireland, BT51 3RP, United Kingdom
Telephone: +44 (0) 28 70 868733

rev.01

PRINCIPAL DISPLAY PANEL
Nicotine compound, solid, n.o.s.
(Nicotine Polacrilex 18%) 
NDC Number: 61252-3002


NICOTINE POLACRILEX 
nicotine polacrilex powder
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61252-3004
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NICOTINE (NICOTINE) NICOTINE 150 g  in 1 kg
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61252-3004-1 5 kg in 1 DRUM None
2 NDC:61252-3004-2 10 kg in 1 DRUM None
3 NDC:61252-3004-3 20 kg in 1 DRUM None
4 NDC:61252-3004-4 25 kg in 1 DRUM None
5 NDC:61252-3004-5 5 kg in 1 BOX None
6 NDC:61252-3004-6 10 kg in 1 BOX None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 02/01/1994

NICOTINE POLACRILEX 
nicotine polacrilex powder
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61252-3003
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NICOTINE (NICOTINE) NICOTINE 200 g  in 1 kg
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61252-3003-1 5 kg in 1 DRUM None
2 NDC:61252-3003-2 10 kg in 1 DRUM None
3 NDC:61252-3003-3 20 kg in 1 DRUM None
4 NDC:61252-3003-4 25 kg in 1 DRUM None
5 NDC:61252-3003-5 5 kg in 1 BOX None
6 NDC:61252-3003-6 10 kg in 1 BOX None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 02/01/1994

NICOTINE POLACRILEX 
nicotine polacrilex powder
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:61252-3002
Route of Administration ORAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
NICOTINE (NICOTINE) NICOTINE 180 g  in 1 kg
Product Characteristics
Color      Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:61252-3002-1 5 kg in 1 DRUM None
2 NDC:61252-3002-2 10 kg in 1 DRUM None
3 NDC:61252-3002-3 20 kg in 1 DRUM None
4 NDC:61252-3002-4 25 kg in 1 DRUM None
5 NDC:61252-3002-5 5 kg in 1 BOX None
6 NDC:61252-3002-6 10 kg in 1 BOX None

Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 02/01/1994

Labeler - Nicobrand LTD (424399871)
Establishment
Name Address ID/FEI Operations
Nicobrand LTD 424399871 API MANUFACTURE

Revised: 07/2010 Nicobrand LTD



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


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