LISINOPRIL - 49999-182-30 - (LISINOPRIL)

Alphabetical Index


Drug Information of LISINOPRIL

Product NDC: 49999-182
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: 49999-182
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077321
Marketing Category: ANDA
Start Marketing Date: 20120327

Package Information of LISINOPRIL

Package NDC: 49999-182-30
Package Description: 30 TABLET in 1 BOTTLE (49999-182-30)

NDC Information of LISINOPRIL

NDC Code 49999-182-30
Proprietary Name LISINOPRIL
Package Description 30 TABLET in 1 BOTTLE (49999-182-30)
Product NDC 49999-182
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LISINOPRIL
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120327
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name LISINOPRIL
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of LISINOPRIL


General Information