lisinopril

Product NDC
70518-4509
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
lisinopril
Dosage form
TABLET
Route
ORAL
Labeler
REMEDYREPACK INC.
Application
ANDA076102
Marketing category
ANDA
Substance
LISINOPRIL
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
70518-4509-090 TABLET in 1 BOTTLE, PLASTIC (70518-4509-0) 2025-10-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
lisinoprilREMEDYREPACK INC.2025-10-21HUMAN PRESCRIPTION DRUG LABEL1