Ibuprofen

Product NDC
71862-007
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Landmark Supply Inc.
Application
ANDA202413
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Historical FDA.report record

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71862-007-01100 TABLET in 1 BOTTLE (71862-007-01) 2017-12-010000-00-00NoCurrent

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USPLandmark Supply Inc.2021-04-29HUMAN PRESCRIPTION DRUG LABEL2