Captopril - 0143-1171-10 - (Captopril)

Alphabetical Index


Drug Information of Captopril

Product NDC: 0143-1171
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: 0143-1171
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074505
Marketing Category: ANDA
Start Marketing Date: 19960213

Package Information of Captopril

Package NDC: 0143-1171-10
Package Description: 1000 TABLET in 1 BOTTLE (0143-1171-10)

NDC Information of Captopril

NDC Code 0143-1171-10
Proprietary Name Captopril
Package Description 1000 TABLET in 1 BOTTLE (0143-1171-10)
Product NDC 0143-1171
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 West-ward Pharmaceutical Corp
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