Home > National Drug Code (NDC) > Metoprolol Tartrate

Metoprolol Tartrate - 54868-2989-2 - (Metoprolol Tartrate)

Alphabetical Index


Drug Information of Metoprolol Tartrate

Product NDC: 54868-2989
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: 54868-2989
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077739
Marketing Category: ANDA
Start Marketing Date: 19940105

Package Information of Metoprolol Tartrate

Package NDC: 54868-2989-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (54868-2989-2)

NDC Information of Metoprolol Tartrate

NDC Code 54868-2989-2
Proprietary Name Metoprolol Tartrate
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (54868-2989-2)
Product NDC 54868-2989
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940105
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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


General Information