ibuprofen

Product NDC
11822-0131
11-digit product format
118220131
Labeler code
11822
Product ID
11822-0131_3fd4732b-a2fc-43c1-9177-a23d944fa93b
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA203599
Marketing category
ANDA
Marketing start
2017-06-16
Marketing end
0000-00-00
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
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0131-1118220131011 BOTTLE in 1 CARTON (11822-0131-1) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2017-06-230000-00-00NoNoCurrent
11822-0131-2118220131021 BOTTLE in 1 CARTON (11822-0131-2) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2017-06-160000-00-00NoNoCurrent
11822-0131-311822013103300 CAPSULE, LIQUID FILLED in 1 BOTTLE (11822-0131-3) 2017-07-110000-00-00NoNoCurrent
11822-0131-4118220131041 BOTTLE in 1 CARTON (11822-0131-4) > 160 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2017-07-110000-00-00NoNoCurrent
11822-0131-5118220131051 BOTTLE in 1 CARTON (11822-0131-5) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2020-03-200000-00-00NoNoCurrent