IBUPROFEN

Product NDC
71335-1503
11-digit product format
713351503
Labeler code
71335
Product ID
71335-1503_840d6421-5e3e-4933-84fb-e5676439b9a0
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
IBUPROFEN
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA090796
Marketing category
ANDA
Marketing start
2015-12-30
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 formatDescriptionMarketing startSampleExclude flagStatus
71335-1503-07133515030021 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0) 2020-02-12NoNoHistorical
71335-1503-17133515030120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1) 2020-02-12NoNoHistorical
71335-1503-27133515030215 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2) 2020-02-12NoNoHistorical
71335-1503-37133515030330 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3) 2020-02-12NoNoHistorical
71335-1503-47133515030440 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4) 2020-02-12NoNoHistorical
71335-1503-57133515030560 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5) 2020-02-12NoNoHistorical
71335-1503-67133515030690 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6) 2020-02-12NoNoHistorical
71335-1503-771335150307120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7) 2020-02-12NoNoHistorical
71335-1503-87133515030850 TABLET, FILM COATED in 1 BOTTLE (71335-1503-8) 2020-02-12NoNoHistorical
71335-1503-971335150309100 TABLET, FILM COATED in 1 BOTTLE (71335-1503-9) 2020-02-12NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
IBUPROFEN 400 MG - 600 MG AND 800 MG TABLETSBryant Ranch Prepack2020-05-27HUMAN PRESCRIPTION DRUG LABEL4