TOPROL - 0186-1090-05 - (Metoprolol succinate)

Alphabetical Index


Drug Information of TOPROL

Product NDC: 0186-1090
Proprietary Name: TOPROL
Non Proprietary Name: Metoprolol succinate
Active Ingredient(s): 50    mg/1 & nbsp;   Metoprolol succinate
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of TOPROL

Product NDC: 0186-1090
Labeler Name: AstraZeneca LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019962
Marketing Category: NDA
Start Marketing Date: 19920201

Package Information of TOPROL

Package NDC: 0186-1090-05
Package Description: 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1090-05)

NDC Information of TOPROL

NDC Code 0186-1090-05
Proprietary Name TOPROL
Package Description 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0186-1090-05)
Product NDC 0186-1090
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 19920201
Marketing Category Name NDA
Labeler Name AstraZeneca LP
Substance Name METOPROLOL SUCCINATE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of TOPROL


General Information