Lisinopril - 68788-9822-6 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 68788-9822
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: 68788-9822
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20120405

Package Information of Lisinopril

Package NDC: 68788-9822-6
Package Description: 60 TABLET in 1 BOTTLE (68788-9822-6)

NDC Information of Lisinopril

NDC Code 68788-9822-6
Proprietary Name Lisinopril
Package Description 60 TABLET in 1 BOTTLE (68788-9822-6)
Product NDC 68788-9822
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120405
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information