Ibuprofen

Product NDC
50090-6677
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
50090-6677-090 TABLET in 1 BOTTLE (50090-6677-0) 2023-09-05NoHistorical
50090-6677-228 TABLET in 1 BOTTLE (50090-6677-2) 2023-09-05NoHistorical

Related DailyMed Labels

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