Ibuprofen

Product NDC
71335-2689
11-digit product format
713352689
Labeler code
71335
Product ID
71335-2689_02d16074-f2b6-4be5-a138-e31fd04f4b9e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA213794
Marketing category
ANDA
Marketing start
2020-05-08
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
71335-2689-07133526890084 TABLET in 1 BOTTLE (71335-2689-0) 84 tablet2025-09-18NoNoHistorical
71335-2689-17133526890120 TABLET in 1 BOTTLE (71335-2689-1) 20 tablet2025-09-18NoNoHistorical
71335-2689-27133526890215 TABLET in 1 BOTTLE (71335-2689-2) 15 tablet2025-09-18NoNoHistorical
71335-2689-37133526890340 TABLET in 1 BOTTLE (71335-2689-3) 40 tablet2025-09-18NoNoHistorical
71335-2689-47133526890421 TABLET in 1 BOTTLE (71335-2689-4) 21 tablet2025-09-18NoNoHistorical
71335-2689-57133526890530 TABLET in 1 BOTTLE (71335-2689-5) 30 tablet2025-09-18NoNoHistorical
71335-2689-67133526890690 TABLET in 1 BOTTLE (71335-2689-6) 90 tablet2025-09-18NoNoHistorical
71335-2689-771335268907100 TABLET in 1 BOTTLE (71335-2689-7) 100 tablet2025-09-18NoNoHistorical
71335-2689-871335268908120 TABLET in 1 BOTTLE (71335-2689-8) 120 tablet2025-09-18NoNoHistorical
71335-2689-97133526890960 TABLET in 1 BOTTLE (71335-2689-9) 60 tablet2025-09-18NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyBryant Ranch Prepack2025-09-18HUMAN PRESCRIPTION DRUG LABEL1