Lisinopril - 21695-329-78 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 21695-329
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 10    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 21695-329
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076059
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril

Package NDC: 21695-329-78
Package Description: 180 TABLET in 1 BOTTLE (21695-329-78)

NDC Information of Lisinopril

NDC Code 21695-329-78
Proprietary Name Lisinopril
Package Description 180 TABLET in 1 BOTTLE (21695-329-78)
Product NDC 21695-329
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 Rebel Distributors Corp
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information