Metoprolol - 25021-303-05 - (metoprolol tartrate)

Alphabetical Index


Drug Information of Metoprolol

Product NDC: 25021-303
Proprietary Name: Metoprolol
Non Proprietary Name: metoprolol tartrate
Active Ingredient(s): 5    mg/5mL & nbsp;   metoprolol tartrate
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Metoprolol

Product NDC: 25021-303
Labeler Name: Sagent Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090317
Marketing Category: ANDA
Start Marketing Date: 20100510

Package Information of Metoprolol

Package NDC: 25021-303-05
Package Description: 10 VIAL in 1 CARTON (25021-303-05) > 5 mL in 1 VIAL

NDC Information of Metoprolol

NDC Code 25021-303-05
Proprietary Name Metoprolol
Package Description 10 VIAL in 1 CARTON (25021-303-05) > 5 mL in 1 VIAL
Product NDC 25021-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20100510
Marketing Category Name ANDA
Labeler Name Sagent Pharmaceuticals
Substance Name METOPROLOL TARTRATE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Metoprolol


General Information