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METOPROLOL SUCCINATE - 49884-405-10 - (Metoprolol succinate)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 49884-405
Proprietary Name: METOPROLOL SUCCINATE
Non Proprietary Name: Metoprolol succinate
Active Ingredient(s): 50    mg/1 & nbsp;   Metoprolol succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 49884-405
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019962
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20070802

Package Information of METOPROLOL SUCCINATE

Package NDC: 49884-405-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-405-10)

NDC Information of METOPROLOL SUCCINATE

NDC Code 49884-405-10
Proprietary Name METOPROLOL SUCCINATE
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (49884-405-10)
Product NDC 49884-405
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20070802
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Par Pharmaceutical Inc.
Substance Name METOPROLOL SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of METOPROLOL SUCCINATE


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