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Metoprolol Succinate - 62037-830-01 - (Metoprolol Succinate)

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Drug Information of Metoprolol Succinate

Product NDC: 62037-830
Proprietary Name: Metoprolol Succinate
Non Proprietary Name: Metoprolol Succinate
Active Ingredient(s): 25    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: 62037-830
Labeler Name: Watson Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077118
Marketing Category: ANDA
Start Marketing Date: 20090804

Package Information of Metoprolol Succinate

Package NDC: 62037-830-01
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-830-01)

NDC Information of Metoprolol Succinate

NDC Code 62037-830-01
Proprietary Name Metoprolol Succinate
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (62037-830-01)
Product NDC 62037-830
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 20090804
Marketing Category Name ANDA
Labeler Name Watson Pharma, Inc.
Substance Name METOPROLOL SUCCINATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Succinate


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