Lisinopril - 53808-0702-1 - (lisinopril)

Alphabetical Index


Drug Information of Lisinopril

Product NDC: 53808-0702
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: 53808-0702
Labeler Name: State of Florida DOH Central Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076071
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Lisinopril

Package NDC: 53808-0702-1
Package Description: 30 TABLET in 1 BLISTER PACK (53808-0702-1)

NDC Information of Lisinopril

NDC Code 53808-0702-1
Proprietary Name Lisinopril
Package Description 30 TABLET in 1 BLISTER PACK (53808-0702-1)
Product NDC 53808-0702
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name lisinopril
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090701
Marketing Category Name ANDA
Labeler Name State of Florida DOH Central Pharmacy
Substance Name LISINOPRIL
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Lisinopril


General Information