Lisinopril - 68084-060-01 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 68084-060
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 5    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 68084-060
Labeler Name: American Health Packaging
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20050922

Package Information of Lisinopril

Package NDC: 68084-060-01
Package Description: 10 BLISTER PACK in 1 CARTON (68084-060-01) > 10 TABLET in 1 BLISTER PACK (68084-060-11)

NDC Information of Lisinopril

NDC Code 68084-060-01
Proprietary Name Lisinopril
Package Description 10 BLISTER PACK in 1 CARTON (68084-060-01) > 10 TABLET in 1 BLISTER PACK (68084-060-11)
Product NDC 68084-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20050922
Marketing Category Name ANDA
Labeler Name American Health Packaging
Substance Name LISINOPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information