Ibuprofen

Product NDC
50090-7283
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
50090-7283-010 TABLET, FILM COATED in 1 BOTTLE (50090-7283-0) 2024-10-08NoHistorical
50090-7283-115 TABLET, FILM COATED in 1 BOTTLE (50090-7283-1) 2024-10-08NoHistorical
50090-7283-230 TABLET, FILM COATED in 1 BOTTLE (50090-7283-2) 2024-10-08NoHistorical
50090-7283-345 TABLET, FILM COATED in 1 BOTTLE (50090-7283-3) 2024-10-08NoHistorical
50090-7283-460 TABLET, FILM COATED in 1 BOTTLE (50090-7283-4) 2024-10-08NoHistorical
50090-7283-5100 TABLET, FILM COATED in 1 BOTTLE (50090-7283-5) 2024-10-08NoHistorical
50090-7283-721 TABLET, FILM COATED in 1 BOTTLE (50090-7283-7) 2024-10-08NoHistorical
50090-7283-812 TABLET, FILM COATED in 1 BOTTLE (50090-7283-8) 2024-10-08NoHistorical
50090-7283-940 TABLET, FILM COATED in 1 BOTTLE (50090-7283-9) 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