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Metoprolol Succinate - 54868-5731-6 - (Metoprolol Succinate)

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Drug Information of Metoprolol Succinate

Product NDC: 54868-5731
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: 54868-5731
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076969
Marketing Category: ANDA
Start Marketing Date: 20100105

Package Information of Metoprolol Succinate

Package NDC: 54868-5731-6
Package Description: 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5731-6)

NDC Information of Metoprolol Succinate

NDC Code 54868-5731-6
Proprietary Name Metoprolol Succinate
Package Description 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5731-6)
Product NDC 54868-5731
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 20100105
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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