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Metoprolol Succinate - 21695-950-90 - (Metoprolol Succinate)

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Drug Information of Metoprolol Succinate

Product NDC: 21695-950
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: 21695-950
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076862
Marketing Category: ANDA
Start Marketing Date: 20090803

Package Information of Metoprolol Succinate

Package NDC: 21695-950-90
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-950-90)

NDC Information of Metoprolol Succinate

NDC Code 21695-950-90
Proprietary Name Metoprolol Succinate
Package Description 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-950-90)
Product NDC 21695-950
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090803
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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