CAPTOPRIL - 64679-904-02 - (CAPTORPIL)

Alphabetical Index


Drug Information of CAPTOPRIL

Product NDC: 64679-904
Proprietary Name: CAPTOPRIL
Non Proprietary Name: CAPTORPIL
Active Ingredient(s): 50    mg/1 & nbsp;   CAPTORPIL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CAPTOPRIL

Product NDC: 64679-904
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074532
Marketing Category: ANDA
Start Marketing Date: 19970328

Package Information of CAPTOPRIL

Package NDC: 64679-904-02
Package Description: 1000 TABLET in 1 BOTTLE (64679-904-02)

NDC Information of CAPTOPRIL

NDC Code 64679-904-02
Proprietary Name CAPTOPRIL
Package Description 1000 TABLET in 1 BOTTLE (64679-904-02)
Product NDC 64679-904
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 USA LLC.
Substance Name CAPTOPRIL
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of CAPTOPRIL


General Information