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metoprolol succinate - 58177-369-11 - (metoprolol succinate)

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Drug Information of metoprolol succinate

Product NDC: 58177-369
Proprietary Name: metoprolol succinate
Non Proprietary Name: metoprolol succinate
Active Ingredient(s): 47.5    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: 58177-369
Labeler Name: Ethex Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077176
Marketing Category: ANDA
Start Marketing Date: 20091101

Package Information of metoprolol succinate

Package NDC: 58177-369-11
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (58177-369-11)

NDC Information of metoprolol succinate

NDC Code 58177-369-11
Proprietary Name metoprolol succinate
Package Description 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (58177-369-11)
Product NDC 58177-369
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 20091101
Marketing Category Name ANDA
Labeler Name Ethex Corporation
Substance Name METOPROLOL SUCCINATE
Strength Number 47.5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of metoprolol succinate


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