TOPROL - 55154-5026-0 - (Metoprolol succinate)

Alphabetical Index


Drug Information of TOPROL

Product NDC: 55154-5026
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: 55154-5026
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019962
Marketing Category: NDA
Start Marketing Date: 20100510

Package Information of TOPROL

Package NDC: 55154-5026-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5026-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of TOPROL

NDC Code 55154-5026-0
Proprietary Name TOPROL
Package Description 10 BLISTER PACK in 1 BAG (55154-5026-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 55154-5026
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Metoprolol succinate
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100510
Marketing Category Name NDA
Labeler Name Cardinal Health
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