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Metoprolol Tartrate - 49349-186-23 - (Metoprolol Tartrate)

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Drug Information of Metoprolol Tartrate

Product NDC: 49349-186
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: 49349-186
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078459
Marketing Category: ANDA
Start Marketing Date: 20110419

Package Information of Metoprolol Tartrate

Package NDC: 49349-186-23
Package Description: 180 TABLET, FILM COATED in 1 VIAL (49349-186-23)

NDC Information of Metoprolol Tartrate

NDC Code 49349-186-23
Proprietary Name Metoprolol Tartrate
Package Description 180 TABLET, FILM COATED in 1 VIAL (49349-186-23)
Product NDC 49349-186
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110419
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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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