CAPTOPRIL - 55648-905-01 - (CAPTORPIL)

Alphabetical Index


Drug Information of CAPTOPRIL

Product NDC: 55648-905
Proprietary Name: CAPTOPRIL
Non Proprietary Name: CAPTORPIL
Active Ingredient(s): 100    mg/1 & nbsp;   CAPTORPIL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CAPTOPRIL

Product NDC: 55648-905
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074532
Marketing Category: ANDA
Start Marketing Date: 19970328

Package Information of CAPTOPRIL

Package NDC: 55648-905-01
Package Description: 100 TABLET in 1 BOTTLE (55648-905-01)

NDC Information of CAPTOPRIL

NDC Code 55648-905-01
Proprietary Name CAPTOPRIL
Package Description 100 TABLET in 1 BOTTLE (55648-905-01)
Product NDC 55648-905
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CAPTORPIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970328
Marketing Category Name ANDA
Labeler Name Wockhardt Limited
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