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METOPROLOL SUCCINATE - 52125-064-02 - (Metoprolol succinate)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 52125-064
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 52125-064
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019962
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20130308

Package Information of METOPROLOL SUCCINATE

Package NDC: 52125-064-02
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-064-02)

NDC Information of METOPROLOL SUCCINATE

NDC Code 52125-064-02
Proprietary Name METOPROLOL SUCCINATE
Package Description 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (52125-064-02)
Product NDC 52125-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130308
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name REMEDYREPACK 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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