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Metoprolol Tartrate - 50436-6578-1 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 50436-6578
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 50436-6578
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078459
Marketing Category: ANDA
Start Marketing Date: 20090315

Package Information of Metoprolol Tartrate

Package NDC: 50436-6578-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (50436-6578-1)

NDC Information of Metoprolol Tartrate

NDC Code 50436-6578-1
Proprietary Name Metoprolol Tartrate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (50436-6578-1)
Product NDC 50436-6578
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20090315
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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