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Metoprolol Tartrate - 13107-064-99 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 13107-064
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: 13107-064
Labeler Name: Aurolife Pharma LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077739
Marketing Category: ANDA
Start Marketing Date: 20100917

Package Information of Metoprolol Tartrate

Package NDC: 13107-064-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99)

NDC Information of Metoprolol Tartrate

NDC Code 13107-064-99
Proprietary Name Metoprolol Tartrate
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (13107-064-99)
Product NDC 13107-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100917
Marketing Category Name ANDA
Labeler Name Aurolife Pharma LLC
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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