CAPTOPRIL - 50436-6104-1 - (CAPTOPRIL)

Alphabetical Index


Drug Information of CAPTOPRIL

Product NDC: 50436-6104
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: 50436-6104
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074532
Marketing Category: ANDA
Start Marketing Date: 19970328

Package Information of CAPTOPRIL

Package NDC: 50436-6104-1
Package Description: 30 TABLET in 1 BOTTLE (50436-6104-1)

NDC Information of CAPTOPRIL

NDC Code 50436-6104-1
Proprietary Name CAPTOPRIL
Package Description 30 TABLET in 1 BOTTLE (50436-6104-1)
Product NDC 50436-6104
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CAPTOPRIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19970328
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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