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Metoprolol Tartrate - 55154-4551-9 - (Metoprolol tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 55154-4551
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: 55154-4551
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 19970701

Package Information of Metoprolol Tartrate

Package NDC: 55154-4551-9
Package Description: 6 BLISTER PACK in 1 CARTON (55154-4551-9) > 5 TABLET in 1 BLISTER PACK

NDC Information of Metoprolol Tartrate

NDC Code 55154-4551-9
Proprietary Name Metoprolol Tartrate
Package Description 6 BLISTER PACK in 1 CARTON (55154-4551-9) > 5 TABLET in 1 BLISTER PACK
Product NDC 55154-4551
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970701
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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