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Metoprolol Tartrate - 76237-208-30 - (Metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 76237-208
Proprietary Name: Metoprolol Tartrate
Non Proprietary Name: Metoprolol tartrate
Active Ingredient(s): 50    mg/1 & nbsp;   Metoprolol tartrate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 76237-208
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 20111004

Package Information of Metoprolol Tartrate

Package NDC: 76237-208-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-208-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Metoprolol Tartrate

NDC Code 76237-208-30
Proprietary Name Metoprolol Tartrate
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-208-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-208
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111004
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name METOPROLOL TARTRATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol Tartrate


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