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METOPROLOL SUCCINATE - 0615-6589-39 - (METOPROLOL SUCCINATE)

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Drug Information of METOPROLOL SUCCINATE

Product NDC: 0615-6589
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, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of METOPROLOL SUCCINATE

Product NDC: 0615-6589
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090615
Marketing Category: ANDA
Start Marketing Date: 20100722

Package Information of METOPROLOL SUCCINATE

Package NDC: 0615-6589-39
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-6589-39)

NDC Information of METOPROLOL SUCCINATE

NDC Code 0615-6589-39
Proprietary Name METOPROLOL SUCCINATE
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-6589-39)
Product NDC 0615-6589
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 20100722
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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


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