Ibuprofen

Product NDC
71610-892
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA075682
Marketing category
ANDA
Substance
IBUPROFEN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
71610-892-5360 TABLET in 1 BOTTLE (71610-892-53) 2025-03-28NoHistorical
71610-892-6090 TABLET in 1 BOTTLE (71610-892-60) 2025-03-28NoHistorical
71610-892-70120 TABLET in 1 BOTTLE (71610-892-70) 2025-03-28NoHistorical
71610-892-80180 TABLET in 1 BOTTLE (71610-892-80) 2025-03-28NoHistorical
71610-892-92270 TABLET in 1 BOTTLE (71610-892-92) 2025-03-28NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
IBU ™ TabletsAphena Pharma Solutions - Tennessee, LLC2025-04-03HUMAN PRESCRIPTION DRUG LABEL1