Ibuprofen

Product NDC
50090-6676
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA213794
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-6676-016 TABLET in 1 BOTTLE (50090-6676-0) 2023-09-05NoHistorical
50090-6676-130 TABLET in 1 BOTTLE (50090-6676-1) 2023-09-05NoHistorical
50090-6676-3100 TABLET in 1 BOTTLE (50090-6676-3) 2023-09-05NoHistorical
50090-6676-420 TABLET in 1 BOTTLE (50090-6676-4) 2023-09-05NoHistorical
50090-6676-860 TABLET in 1 BOTTLE (50090-6676-8) 2023-09-05NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyA-S Medication Solutions2023-09-06Human Prescription Drug Label6