lisinopril - 49999-183-90 - (lisinopril)

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Drug Information of lisinopril

Product NDC: 49999-183
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: 49999-183
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075994
Marketing Category: ANDA
Start Marketing Date: 20110719

Package Information of lisinopril

Package NDC: 49999-183-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (49999-183-90)

NDC Information of lisinopril

NDC Code 49999-183-90
Proprietary Name lisinopril
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (49999-183-90)
Product NDC 49999-183
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110719
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
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