Lisinopril - 68387-521-10 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 68387-521
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: 68387-521
Labeler Name: Keltman Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20101210

Package Information of Lisinopril

Package NDC: 68387-521-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (68387-521-10)

NDC Information of Lisinopril

NDC Code 68387-521-10
Proprietary Name Lisinopril
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (68387-521-10)
Product NDC 68387-521
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101210
Marketing Category Name ANDA
Labeler Name Keltman Pharmaceuticals Inc.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information