LISINOPRIL - 10544-239-30 - (LISINOPRIL)

Alphabetical Index


Drug Information of LISINOPRIL

Product NDC: 10544-239
Proprietary Name: LISINOPRIL
Non Proprietary Name: LISINOPRIL
Active Ingredient(s): 20    mg/1 & nbsp;   LISINOPRIL
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of LISINOPRIL

Product NDC: 10544-239
Labeler Name: Blenheim Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20091216

Package Information of LISINOPRIL

Package NDC: 10544-239-30
Package Description: 30 TABLET in 1 BOTTLE (10544-239-30)

NDC Information of LISINOPRIL

NDC Code 10544-239-30
Proprietary Name LISINOPRIL
Package Description 30 TABLET in 1 BOTTLE (10544-239-30)
Product NDC 10544-239
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LISINOPRIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091216
Marketing Category Name ANDA
Labeler Name Blenheim Pharmacal, Inc.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of LISINOPRIL


General Information