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Metoprolol Tartrate - 55154-5356-0 - (metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 55154-5356
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: 55154-5356
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076704
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Metoprolol Tartrate

Package NDC: 55154-5356-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5356-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Metoprolol Tartrate

NDC Code 55154-5356-0
Proprietary Name Metoprolol Tartrate
Package Description 10 BLISTER PACK in 1 BAG (55154-5356-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5356
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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