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Metoprolol Tartrate - 0378-0047-02 - (metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0378-0047
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: metoprolol tartrate
Active Ingredient(s): 100    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: 0378-0047
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076704
Marketing Category: ANDA
Start Marketing Date: 20120502

Package Information of Metoprolol Tartrate

Package NDC: 0378-0047-02
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0047-02)

NDC Information of Metoprolol Tartrate

NDC Code 0378-0047-02
Proprietary Name Metoprolol Tartrate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-0047-02)
Product NDC 0378-0047
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120502
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name METOPROLOL TARTRATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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