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Metoprolol succinate - 55111-466-30 - (Metoprolol succinate)

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Drug Information of Metoprolol succinate

Product NDC: 55111-466
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: 55111-466
Labeler Name: Dr. Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090617
Marketing Category: ANDA
Start Marketing Date: 20120910

Package Information of Metoprolol succinate

Package NDC: 55111-466-30
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-466-30)

NDC Information of Metoprolol succinate

NDC Code 55111-466-30
Proprietary Name Metoprolol succinate
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55111-466-30)
Product NDC 55111-466
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120910
Marketing Category Name ANDA
Labeler Name Dr. Reddy's Laboratories Limited
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


General Information