Home > National Drug Code (NDC) > Metoprolol Tartrate

Metoprolol Tartrate - 49349-603-24 - (Metoprolol Tartrate)

Alphabetical Index


Drug Information of Metoprolol Tartrate

Product NDC: 49349-603
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
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol Tartrate

Product NDC: 49349-603
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078459
Marketing Category: ANDA
Start Marketing Date: 20111102

Package Information of Metoprolol Tartrate

Package NDC: 49349-603-24
Package Description: 200 TABLET in 1 CANISTER (49349-603-24)

NDC Information of Metoprolol Tartrate

NDC Code 49349-603-24
Proprietary Name Metoprolol Tartrate
Package Description 200 TABLET in 1 CANISTER (49349-603-24)
Product NDC 49349-603
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol Tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20111102
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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


General Information