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METOPROLOL SUCCINATE - 55648-736-09 - (METOPROLOL SUCCINATE)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 55648-736
Proprietary Name: METOPROLOL SUCCINATE
Non Proprietary Name: METOPROLOL SUCCINATE
Active Ingredient(s): 100    mg/1 & nbsp;   METOPROLOL SUCCINATE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 55648-736
Labeler Name: WOCKHARDT LIMITED
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090615
Marketing Category: ANDA
Start Marketing Date: 20100722

Package Information of METOPROLOL SUCCINATE

Package NDC: 55648-736-09
Package Description: 12 BOTTLE in 1 CARTON (55648-736-09) > 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of METOPROLOL SUCCINATE

NDC Code 55648-736-09
Proprietary Name METOPROLOL SUCCINATE
Package Description 12 BOTTLE in 1 CARTON (55648-736-09) > 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 55648-736
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name METOPROLOL SUCCINATE
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100722
Marketing Category Name ANDA
Labeler Name WOCKHARDT LIMITED
Substance Name METOPROLOL SUCCINATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of METOPROLOL SUCCINATE


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