Lisinopril - 65862-040-05 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 65862-040
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: 65862-040
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077622
Marketing Category: ANDA
Start Marketing Date: 20060222

Package Information of Lisinopril

Package NDC: 65862-040-05
Package Description: 500 TABLET in 1 BOTTLE (65862-040-05)

NDC Information of Lisinopril

NDC Code 65862-040-05
Proprietary Name Lisinopril
Package Description 500 TABLET in 1 BOTTLE (65862-040-05)
Product NDC 65862-040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060222
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information