Lisinopril - 76237-199-30 - (lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 76237-199
Proprietary Name: Lisinopril
Non Proprietary Name: lisinopril
Active Ingredient(s): 40    mg/1 & nbsp;   lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 76237-199
Labeler Name: McKesson Contract Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20110916

Package Information of Lisinopril

Package NDC: 76237-199-30
Package Description: 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-199-30) > 5 TABLET in 1 BLISTER PACK

NDC Information of Lisinopril

NDC Code 76237-199-30
Proprietary Name Lisinopril
Package Description 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-199-30) > 5 TABLET in 1 BLISTER PACK
Product NDC 76237-199
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110916
Marketing Category Name ANDA
Labeler Name McKesson Contract Packaging
Substance Name LISINOPRIL
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information