Lisinopril - 49349-548-30 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 49349-548
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: 49349-548
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076059
Marketing Category: ANDA
Start Marketing Date: 20110929

Package Information of Lisinopril

Package NDC: 49349-548-30
Package Description: 400 TABLET in 1 CANISTER (49349-548-30)

NDC Information of Lisinopril

NDC Code 49349-548-30
Proprietary Name Lisinopril
Package Description 400 TABLET in 1 CANISTER (49349-548-30)
Product NDC 49349-548
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110929
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information