Lisinopril - 50436-2000-1 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 50436-2000
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: 50436-2000
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril

Package NDC: 50436-2000-1
Package Description: 30 TABLET in 1 BOTTLE (50436-2000-1)

NDC Information of Lisinopril

NDC Code 50436-2000-1
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE (50436-2000-1)
Product NDC 50436-2000
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020701
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name LISINOPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information