Ibuprofen

Product NDC
11822-9380
11-digit product format
118229380
Labeler code
11822
Product ID
11822-9380_99984265-ee60-4b51-810e-614440e9d269
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA074916
Marketing category
ANDA
Marketing start
2022-02-04
Marketing end
0000-00-00
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
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-9380IBUPROFEN CHILDRENS (IBUPROFEN) SUSPENSION [RITE AID CORPORATION]2Legacy NDC20241109_b478cb07-0ea9-4b85-8082-cdb7145c20eb.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-9380-4118229380041 BOTTLE in 1 CARTON (11822-9380-4) > 118 mL in 1 BOTTLE1 bottle2022-02-040000-00-00NoNoCurrent