Lisinopril - 64679-941-03 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 64679-941
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: 64679-941
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20070419

Package Information of Lisinopril

Package NDC: 64679-941-03
Package Description: 10 BLISTER PACK in 1 CARTON (64679-941-03) > 10 TABLET in 1 BLISTER PACK

NDC Information of Lisinopril

NDC Code 64679-941-03
Proprietary Name Lisinopril
Package Description 10 BLISTER PACK in 1 CARTON (64679-941-03) > 10 TABLET in 1 BLISTER PACK
Product NDC 64679-941
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070419
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information