Label: DIGOXIN tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-000-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 0527-1325
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 16, 2014
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PRINCIPAL DISPLAY PANEL
NDC: 51655-000-52
MFG: 0527-1325-10
Digoxin 0.25 MG
30 Tablets
RX only
Lot# NW41860001
Exp. Date: 12/2015
Each tablet contains Digoxin, USP...0.25mg
Dosage: See package insert
Store at 68 to 77 degrees F.
Store in a tight, light resistant container (See USP).
Keep out of the reach of children.
Mfg: By: Jerome Stevens Pharmaceuticals Inc. Bohemia, NY 11716
MFG for: Lannett Co. Inc. Philadelphia, PA 19136 Lot#037213
Repacked by Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
DIGOXIN
digoxin tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-000(NDC:0527-1325) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIGOXIN (UNII: 73K4184T59) (DIGOXIN - UNII:73K4184T59) DIGOXIN 0.25 mg in 30 Product Characteristics Color white Score no score Shape ROUND Size 7mm Flavor Imprint Code JSP545 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-000-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076268 05/16/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-000)