Label: METOPROLOL SUCCINATE tablet, film coated, extended release
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-580-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 62037-831
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 7, 2014
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PRINCIPAL DISPLAY PANEL
NDC: 51655-580-52
MFG: 62037-0831-10
Metoprolol Succinate ER 50 MG
30 Tablets
Rx Only
Lot# NW45880001
Exp: Date: 06/2015
Each tablet contains: 47.5 mg metoprolol succinate equivalent
to 50mg metoprolol tartate, USP
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: Watson Laboratories, Inc Corona, CA 92880 USA
Distributed by: Watson Pharma, Incc Lot: 847064A
Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
METOPROLOL SUCCINATE
metoprolol succinate tablet, film coated, extended releaseProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-580(NDC:62037-831) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METOPROLOL SUCCINATE (UNII: TH25PD4CCB) (METOPROLOL - UNII:GEB06NHM23) METOPROLOL TARTRATE 50 mg in 30 Product Characteristics Color white Score no score Shape ROUND Size 9mm Flavor Imprint Code 831 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-580-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076862 05/07/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-580)