Lisinopril - 54458-996-10 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 54458-996
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: 54458-996
Labeler Name: International Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20080201

Package Information of Lisinopril

Package NDC: 54458-996-10
Package Description: 30 TABLET in 1 BLISTER PACK (54458-996-10)

NDC Information of Lisinopril

NDC Code 54458-996-10
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BLISTER PACK (54458-996-10)
Product NDC 54458-996
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080201
Marketing Category Name ANDA
Labeler Name International Labs, Inc.
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information