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Metoprolol Succinate - 60429-142-10 - (Metoprolol Succinate)

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Drug Information of Metoprolol Succinate

Product NDC: 60429-142
Proprietary Name: Metoprolol Succinate
Non Proprietary Name: Metoprolol Succinate
Active Ingredient(s): 200    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: 60429-142
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077298
Marketing Category: ANDA
Start Marketing Date: 20100415

Package Information of Metoprolol Succinate

Package NDC: 60429-142-10
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-142-10)

NDC Information of Metoprolol Succinate

NDC Code 60429-142-10
Proprietary Name Metoprolol Succinate
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (60429-142-10)
Product NDC 60429-142
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 Golden State Medical Supply, Inc.
Substance Name METOPROLOL SUCCINATE
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Succinate


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