CAPTOPRIL - 68788-9721-1 - (CAPTORPIL)

Alphabetical Index


Drug Information of CAPTOPRIL

Product NDC: 68788-9721
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: 68788-9721
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074532
Marketing Category: ANDA
Start Marketing Date: 20121213

Package Information of CAPTOPRIL

Package NDC: 68788-9721-1
Package Description: 100 TABLET in 1 BOTTLE (68788-9721-1)

NDC Information of CAPTOPRIL

NDC Code 68788-9721-1
Proprietary Name CAPTOPRIL
Package Description 100 TABLET in 1 BOTTLE (68788-9721-1)
Product NDC 68788-9721
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CAPTORPIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20121213
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc.
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