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Metoprolol Tartrate - 0093-0733-01 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 0093-0733
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: 0093-0733
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074141
Marketing Category: ANDA
Start Marketing Date: 19950406

Package Information of Metoprolol Tartrate

Package NDC: 0093-0733-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0733-01)

NDC Information of Metoprolol Tartrate

NDC Code 0093-0733-01
Proprietary Name Metoprolol Tartrate
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0733-01)
Product NDC 0093-0733
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950406
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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