Ibuprofen

Product NDC
71335-2682
11-digit product format
713352682
Labeler code
71335
Product ID
71335-2682_e1aa3e81-8aa9-445a-921d-f7f3d2712fd6
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
400 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

Additional Listing Data

Finished product
Yes
Brand name base
Ibuprofen
Listing expiration
2026-12-31

Related Records

Active Ingredients

IngredientStrength
IBUPROFEN400 mg/1

Harmonized Identifiers

FieldValues
UniiWK2XYI10QM
Rxcui197805

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
WK2XYI10QMIBUPROFEN15687-27-1IBUPROFEN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2682-17133526820120 TABLET in 1 BOTTLE (71335-2682-1) 20 tablet2025-09-17NoNoHistorical
71335-2682-27133526820230 TABLET in 1 BOTTLE (71335-2682-2) 30 tablet2025-09-17NoNoHistorical
71335-2682-37133526820340 TABLET in 1 BOTTLE (71335-2682-3) 40 tablet2025-09-17NoNoHistorical
71335-2682-47133526820460 TABLET in 1 BOTTLE (71335-2682-4) 60 tablet2025-09-17NoNoHistorical
71335-2682-57133526820590 TABLET in 1 BOTTLE (71335-2682-5) 90 tablet2025-09-17NoNoHistorical
71335-2682-671335268206120 TABLET in 1 BOTTLE (71335-2682-6) 120 tablet2025-09-17NoNoHistorical
71335-2682-771335268207100 TABLET in 1 BOTTLE (71335-2682-7) 100 tablet2025-09-17NoNoHistorical
71335-2682-87133526820821 TABLET in 1 BOTTLE (71335-2682-8) 21 tablet2025-09-17NoNoHistorical
71335-2682-97133526820915 TABLET in 1 BOTTLE (71335-2682-9) 15 tablet2025-09-17NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Ibuprofen Tablets, USP Rx onlyBryant Ranch Prepack2025-09-17HUMAN PRESCRIPTION DRUG LABEL1