Lisinopril - 63629-2935-1 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 63629-2935
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: 63629-2935
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20020701

Package Information of Lisinopril

Package NDC: 63629-2935-1
Package Description: 30 TABLET in 1 BOTTLE (63629-2935-1)

NDC Information of Lisinopril

NDC Code 63629-2935-1
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE (63629-2935-1)
Product NDC 63629-2935
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 Bryant Ranch Prepack
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