Ibuprofen

Product NDC
11822-1761
11-digit product format
118221761
Labeler code
11822
Product ID
11822-1761_8ffbff80-10e3-41eb-aaf7-d90c47e09f40
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA074916
Marketing category
ANDA
Marketing start
2018-02-28
Marketing end
0000-00-00
Substance
IBUPROFEN
Active strength
100 mg/5mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
11822-1761-42023-10-31C16284748780-1f386c64a-2d29-0266-e053-dadaa90a7c1ad001c3dd-cfa0-4aa0-a9bb-9c4752fffcd2
11822-1761-42023-01-30C16284748780-1f386c64a-2d29-0266-e053-dadaa90a7c1ad001c3dd-cfa0-4aa0-a9bb-9c4752fffcd2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-1761-4118221761041 BOTTLE in 1 CARTON (11822-1761-4) > 118 mL in 1 BOTTLE1 bottle2018-02-280000-00-00NoNoCurrent