Lisinopril - 63629-1761-2 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 63629-1761
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 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: 63629-1761
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20051117

Package Information of Lisinopril

Package NDC: 63629-1761-2
Package Description: 90 TABLET in 1 BOTTLE (63629-1761-2)

NDC Information of Lisinopril

NDC Code 63629-1761-2
Proprietary Name Lisinopril
Package Description 90 TABLET in 1 BOTTLE (63629-1761-2)
Product NDC 63629-1761
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20051117
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name LISINOPRIL
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information