Lisinopril - 51138-065-30 - (Lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 51138-065
Proprietary Name: Lisinopril
Non Proprietary Name: Lisinopril
Active Ingredient(s): 10    mg/1 & nbsp;   Lisinopril
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Lisinopril

Product NDC: 51138-065
Labeler Name: Med-Health Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076063
Marketing Category: ANDA
Start Marketing Date: 20110105

Package Information of Lisinopril

Package NDC: 51138-065-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (51138-065-30)

NDC Information of Lisinopril

NDC Code 51138-065-30
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (51138-065-30)
Product NDC 51138-065
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110105
Marketing Category Name ANDA
Labeler Name Med-Health Pharma, LLC
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA]

Complete Information of Lisinopril


General Information