ibuprofen

Product NDC
71335-2068
11-digit product format
713352068
Labeler code
71335
Product ID
71335-2068_2c91e959-d2c7-48ce-a4a5-6c540fb90895
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA072096
Marketing category
ANDA
Marketing start
1994-08-16
Substance
IBUPROFEN
Active strength
200 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 formatDescriptionMarketing startSampleExclude flagStatus
71335-2068-07133520680090 TABLET, FILM COATED in 1 BOTTLE (71335-2068-0) 2022-03-29NoNoHistorical
71335-2068-17133520680120 TABLET, FILM COATED in 1 BOTTLE (71335-2068-1) 2022-03-29NoNoHistorical
71335-2068-27133520680215 TABLET, FILM COATED in 1 BOTTLE (71335-2068-2) 2022-03-29NoNoHistorical
71335-2068-37133520680330 TABLET, FILM COATED in 1 BOTTLE (71335-2068-3) 2022-03-29NoNoHistorical
71335-2068-471335206804100 TABLET, FILM COATED in 1 BOTTLE (71335-2068-4) 2022-03-29NoNoHistorical
71335-2068-57133520680560 TABLET, FILM COATED in 1 BOTTLE (71335-2068-5) 2022-03-29NoNoHistorical
71335-2068-67133520680650 TABLET, FILM COATED in 1 BOTTLE (71335-2068-6) 2022-03-29NoNoHistorical
71335-2068-77133520680740 TABLET, FILM COATED in 1 BOTTLE (71335-2068-7) 2022-03-29NoNoHistorical
71335-2068-87133520680810 TABLET, FILM COATED in 1 BOTTLE (71335-2068-8) 2022-03-29NoNoHistorical
71335-2068-97133520680956 TABLET, FILM COATED in 1 BOTTLE (71335-2068-9) 2022-03-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Major Pharmaceuticals Ibuprofen Tablets, 200mg Drug FactsBryant Ranch Prepack2025-08-20HUMAN OTC DRUG LABEL102