Ibuprofen

Product NDC
50090-7288
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA202413
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
50090-7288-010 TABLET, FILM COATED in 1 BOTTLE (50090-7288-0) 2024-10-08NoHistorical
50090-7288-216 TABLET, FILM COATED in 1 BOTTLE (50090-7288-2) 2024-10-08NoHistorical
50090-7288-330 TABLET, FILM COATED in 1 BOTTLE (50090-7288-3) 2024-10-08NoHistorical
50090-7288-460 TABLET, FILM COATED in 1 BOTTLE (50090-7288-4) 2024-10-08NoHistorical
50090-7288-5100 TABLET, FILM COATED in 1 BOTTLE (50090-7288-5) 2024-10-08NoHistorical
50090-7288-740 TABLET, FILM COATED in 1 BOTTLE (50090-7288-7) 2024-10-08NoHistorical
50090-7288-820 TABLET, FILM COATED in 1 BOTTLE (50090-7288-8) 2024-10-08NoHistorical
50090-7288-924 TABLET, FILM COATED in 1 BOTTLE (50090-7288-9) 2024-10-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP 400 mg, 600 mg and 800 mgA-S Medication Solutions2024-10-10HUMAN PRESCRIPTION DRUG LABEL1