Label: CARVEDILOL tablet, film coated
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-002-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 0378-3633
- Category: HUMAN PRESCRIPTION DRUG LABEL
Drug Label Information
Updated May 16, 2014
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PRINCIPAL DISPLAY PANEL
NDC: 51655-002-52
MFG: 0378-3633-01
Carvedilol 12.5 MG
30 Tablets
RX only
Lot#: NW07880001
Exp. Date: 1/2015
Each film-coated tablet contains: Carvedilol, USP...12.5mg
Dosage: See package insert
Store at 68 to 77 degrees F.
Protect from moisture.
Store in a tight, light-resistant container (See USP).
Keep out of the reach of children.
Mfg. by: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA Lot# 3044836
Repackaged By: Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
CARVEDILOL
carvedilol tablet, film coatedProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-002(NDC:0378-3633) Route of Administration Oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CARVEDILOL (UNII: 0K47UL67F2) (CARVEDILOL - UNII:0K47UL67F2) CARVEDILOL 12.5 mg in 30 Product Characteristics Color white Score no score Shape ROUND Size 8mm Flavor Imprint Code M;C33 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-002-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077316 05/16/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-002)