Ibuprofen

Product NDC
71610-891
11-digit product format
716100891
Labeler code
71610
Product ID
71610-891_31e6006b-b875-9bed-e063-6394a90aaa66
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA075682
Marketing category
ANDA
Marketing start
2009-06-10
Substance
IBUPROFEN
Active strength
600 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WK2XYI10QMIBUPROFEN15687-27-1IBUPROFEN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-891-537161008915360 TABLET in 1 BOTTLE (71610-891-53) 60 tablet2025-03-28NoNoHistorical
71610-891-607161008916090 TABLET in 1 BOTTLE (71610-891-60) 90 tablet2025-03-28NoNoHistorical
71610-891-7071610089170120 TABLET in 1 BOTTLE (71610-891-70) 120 tablet2025-03-28NoNoHistorical
71610-891-8071610089180180 TABLET in 1 BOTTLE (71610-891-80) 180 tablet2025-03-28NoNoHistorical
71610-891-9271610089192270 TABLET in 1 BOTTLE (71610-891-92) 270 tablet2025-03-28NoNoHistorical

Related DailyMed Labels

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