Captopril - 55154-0689-0 - (Captopril)

Alphabetical Index


Drug Information of Captopril

Product NDC: 55154-0689
Proprietary Name: Captopril
Non Proprietary Name: Captopril
Active Ingredient(s): 12.5    mg/1 & nbsp;   Captopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Captopril

Product NDC: 55154-0689
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074505
Marketing Category: ANDA
Start Marketing Date: 20040216

Package Information of Captopril

Package NDC: 55154-0689-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0689-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Captopril

NDC Code 55154-0689-0
Proprietary Name Captopril
Package Description 10 BLISTER PACK in 1 BAG (55154-0689-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0689
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Captopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040216
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name CAPTOPRIL
Strength Number 12.5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Captopril


General Information