Lopressor - 30698-459-01 - (metoprolol tartrate)

Alphabetical Index


Drug Information of Lopressor

Product NDC: 30698-459
Proprietary Name: Lopressor
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 Lopressor

Product NDC: 30698-459
Labeler Name: Validus Pharmaceuticals LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017963
Marketing Category: NDA
Start Marketing Date: 19780115

Package Information of Lopressor

Package NDC: 30698-459-01
Package Description: 100 TABLET in 1 BOTTLE (30698-459-01)

NDC Information of Lopressor

NDC Code 30698-459-01
Proprietary Name Lopressor
Package Description 100 TABLET in 1 BOTTLE (30698-459-01)
Product NDC 30698-459
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name metoprolol tartrate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19780115
Marketing Category Name NDA
Labeler Name Validus Pharmaceuticals LLC
Substance Name METOPROLOL TARTRATE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Lopressor


General Information