childrens ibuprofen

Product NDC
11822-1685
11-digit product format
118221685
Labeler code
11822
Product ID
11822-1685_53a8d4e1-2645-4aa7-b7bd-9251db772186
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA074937
Marketing category
ANDA
Marketing start
2023-04-07
Substance
IBUPROFEN
Active strength
100 mg/5mL
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
11822-1685-0118221685001 BOTTLE in 1 CARTON (11822-1685-0) / 120 mL in 1 BOTTLE1 bottle2023-04-07NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Rite Aid Corporation Children’s Ibuprofen Drug FactsRite Aid Corporation2025-04-18HUMAN OTC DRUG LABEL3