Lisinopril - 0615-7639-31 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 0615-7639
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 2.5    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 0615-7639
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078402
Marketing Category: ANDA
Start Marketing Date: 20070419

Package Information of Lisinopril

Package NDC: 0615-7639-31
Package Description: 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-7639-31)

NDC Information of Lisinopril

NDC Code 0615-7639-31
Proprietary Name Lisinopril
Package Description 31 TABLET, FILM COATED in 1 BLISTER PACK (0615-7639-31)
Product NDC 0615-7639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070419
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
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