Ibuprofen

Product NDC
50090-7274
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA209207
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7274-01 BOTTLE in 1 CARTON (50090-7274-0) / 120 mL in 1 BOTTLE2024-10-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
IbuprofenA-S Medication Solutions2024-10-14HUMAN OTC DRUG LABEL1