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Metoprolol Succinate - 63629-4387-2 - (Metoprolol Succinate)

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Drug Information of Metoprolol Succinate

Product NDC: 63629-4387
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Succinate

Product NDC: 63629-4387
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077298
Marketing Category: ANDA
Start Marketing Date: 20100415

Package Information of Metoprolol Succinate

Package NDC: 63629-4387-2
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4387-2)

NDC Information of Metoprolol Succinate

NDC Code 63629-4387-2
Proprietary Name Metoprolol Succinate
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-4387-2)
Product NDC 63629-4387
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100415
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
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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