Captopril - 63629-1706-3 - (Captopril)

Alphabetical Index


Drug Information of Captopril

Product NDC: 63629-1706
Proprietary Name: Captopril
Non Proprietary Name: Captopril
Active Ingredient(s): 100    mg/1 & nbsp;   Captopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Captopril

Product NDC: 63629-1706
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074505
Marketing Category: ANDA
Start Marketing Date: 19960213

Package Information of Captopril

Package NDC: 63629-1706-3
Package Description: 100 TABLET in 1 BOTTLE (63629-1706-3)

NDC Information of Captopril

NDC Code 63629-1706-3
Proprietary Name Captopril
Package Description 100 TABLET in 1 BOTTLE (63629-1706-3)
Product NDC 63629-1706
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Captopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960213
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CAPTOPRIL
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Captopril


General Information