Lisinopril - 0172-3757-10 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 0172-3757
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 2.5    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 0172-3757
Labeler Name: IVAX Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075752
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril

Package NDC: 0172-3757-10
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-3757-10) > 1 TABLET in 1 BLISTER PACK (0172-3757-00)

NDC Information of Lisinopril

NDC Code 0172-3757-10
Proprietary Name Lisinopril
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (0172-3757-10) > 1 TABLET in 1 BLISTER PACK (0172-3757-00)
Product NDC 0172-3757
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020701
Marketing Category Name ANDA
Labeler Name IVAX Pharmaceuticals, Inc.
Substance Name LISINOPRIL
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information