Lisinopril - 68180-517-02 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 68180-517
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 40    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 68180-517
Labeler Name: Lupin Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20060113

Package Information of Lisinopril

Package NDC: 68180-517-02
Package Description: 500 TABLET in 1 BOTTLE (68180-517-02)

NDC Information of Lisinopril

NDC Code 68180-517-02
Proprietary Name Lisinopril
Package Description 500 TABLET in 1 BOTTLE (68180-517-02)
Product NDC 68180-517
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060113
Marketing Category Name ANDA
Labeler Name Lupin Pharmaceuticals, Inc.
Substance Name LISINOPRIL
Strength Number 40
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information