Lisinopril - 24236-615-20 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 24236-615
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 10    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 24236-615
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20130520

Package Information of Lisinopril

Package NDC: 24236-615-20
Package Description: 100 TABLET in 1 VIAL (24236-615-20)

NDC Information of Lisinopril

NDC Code 24236-615-20
Proprietary Name Lisinopril
Package Description 100 TABLET in 1 VIAL (24236-615-20)
Product NDC 24236-615
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130520
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information