Lisinopril - 63739-350-10 - (Lisinopril)

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Drug Information of Lisinopril

Product NDC: 63739-350
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: 63739-350
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076059
Marketing Category: ANDA
Start Marketing Date: 20070924

Package Information of Lisinopril

Package NDC: 63739-350-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-350-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Lisinopril

NDC Code 63739-350-10
Proprietary Name Lisinopril
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-350-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-350
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070924
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
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