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Metoprolol Tartrate - 0615-6547-39 - (metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0615-6547
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: metoprolol tartrate
Active Ingredient(s): 25    mg/1 & nbsp;   metoprolol tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 0615-6547
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076704
Marketing Category: ANDA
Start Marketing Date: 20110505

Package Information of Metoprolol Tartrate

Package NDC: 0615-6547-39
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6547-39)

NDC Information of Metoprolol Tartrate

NDC Code 0615-6547-39
Proprietary Name Metoprolol Tartrate
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-6547-39)
Product NDC 0615-6547
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110505
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name METOPROLOL TARTRATE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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