pain relief

Product NDC
79481-0423
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Meijer, Inc.
Application
ANDA072096
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
79481-0423-01 BOTTLE in 1 CARTON (79481-0423-0) / 24 TABLET, FILM COATED in 1 BOTTLE2024-08-26NoHistorical
79481-0423-11 BOTTLE in 1 CARTON (79481-0423-1) / 50 TABLET, FILM COATED in 1 BOTTLE2024-08-05NoHistorical
79481-0423-2500 TABLET, FILM COATED in 1 BOTTLE (79481-0423-2) 2024-09-30NoHistorical
79481-0423-31 BOTTLE in 1 CARTON (79481-0423-3) / 100 TABLET, FILM COATED in 1 BOTTLE2024-07-15NoHistorical
79481-0423-42 BOTTLE in 1 CARTON (79481-0423-4) / 100 TABLET, FILM COATED in 1 BOTTLE2024-07-22NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Meijer Distribution, Inc. Pain Relief Drug FactsMeijer, Inc.2025-09-19HUMAN OTC DRUG LABEL2