Lisinopril - 49349-016-02 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 49349-016
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: 49349-016
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20100916

Package Information of Lisinopril

Package NDC: 49349-016-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-016-02)

NDC Information of Lisinopril

NDC Code 49349-016-02
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BLISTER PACK (49349-016-02)
Product NDC 49349-016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100916
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LISINOPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information