Home > National Drug Code (NDC) > Metoprolol Tartrate

Metoprolol Tartrate - 52125-521-23 - (Metoprolol tartrate)

Alphabetical Index


Drug Information of Metoprolol Tartrate

Product NDC: 52125-521
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
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 52125-521
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074644
Marketing Category: ANDA
Start Marketing Date: 20130523

Package Information of Metoprolol Tartrate

Package NDC: 52125-521-23
Package Description: 180 TABLET in 1 VIAL (52125-521-23)

NDC Information of Metoprolol Tartrate

NDC Code 52125-521-23
Proprietary Name Metoprolol Tartrate
Package Description 180 TABLET in 1 VIAL (52125-521-23)
Product NDC 52125-521
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130523
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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