IBU

Product NDC
71610-550
11-digit product format
716100550
Labeler code
71610
Product ID
71610-550_19cc7ade-51b3-44f2-9bb1-a7a22909af97
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
2001-11-14
Substance
IBUPROFEN
Active strength
800 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
71610-550-607161005506090 TABLET in 1 BOTTLE (71610-550-60) 90 tablet2021-05-01NoNoHistorical
71610-550-8071610055080180 TABLET in 1 BOTTLE (71610-550-80) 180 tablet2021-05-01NoNoHistorical
71610-550-9271610055092270 TABLET in 1 BOTTLE (71610-550-92) 270 tablet2021-05-01NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
IBU ™ TabletsAphena Pharma Solutions - Tennessee, LLC2021-05-24HUMAN PRESCRIPTION DRUG LABEL1