Lisinopril - 0615-5531-31 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 0615-5531
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 20    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 0615-5531
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075752
Marketing Category: ANDA
Start Marketing Date: 20100420

Package Information of Lisinopril

Package NDC: 0615-5531-31
Package Description: 31 TABLET in 1 BLISTER PACK (0615-5531-31)

NDC Information of Lisinopril

NDC Code 0615-5531-31
Proprietary Name Lisinopril
Package Description 31 TABLET in 1 BLISTER PACK (0615-5531-31)
Product NDC 0615-5531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100420
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information