FDA.reportPublic FDA data

IBUPROFEN

Product NDC
11822-7891
11-digit product format
118227891
Labeler code
11822
Product ID
11822-7891_d4c0db96-297e-6de5-e053-2995a90a7028
Type
HUMAN OTC DRUG
Nonproprietary name
IBUPROFEN
Dosage form
TABLET, COATED
Route
ORAL
Labeler
RITE AID CORPORATION
Application
ANDA091239
Marketing category
ANDA
Marketing start
2020-06-01
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
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN200 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui310965

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
1e73f975-1ce7-705e-2bcf-788b1b5e24baProduct name520251124
16cde546-8deb-4df2-a072-dab5566ede95Product name120231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015Product name420230808
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
61c18d4e-b552-5478-8fc0-df38b93e3100Product name120140508
7b2938c9-7eb7-e312-ae90-f54f4240361eProduct name120140508
997601aa-bb5f-6971-6b90-a21132c12c7bProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11822-7891-2IBUPROFEN50 in 1 BOTTLETABLET, COATED503
11822-7891-5IBUPROFEN100 in 1 BOTTLETABLET, COATED1003
11822-7891-9IBUPROFEN500 in 1 BOTTLETABLET, COATED5003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7891IBUPROFEN TABLET, COATED [RITE AID CORPORATION]3Current NDC, Legacy NDC, 3 package rows20220105_a7aa790a-6d6c-7929-e053-2995a90a1cf8.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSNa7aa790a-6d6c-7929-e053-2995a90a1cf83
310965ibuprofen 200 MG Oral TabletSCDa7aa790a-6d6c-7929-e053-2995a90a1cf83
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSYa7aa790a-6d6c-7929-e053-2995a90a1cf83

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11822-7891-21182278910250 TABLET, COATED in 1 BOTTLE (11822-7891-2) 2020-06-010000-00-00NoNoCurrent
11822-7891-511822789105100 TABLET, COATED in 1 BOTTLE (11822-7891-5) 2020-06-010000-00-00NoNoCurrent
11822-7891-911822789109500 TABLET, COATED in 1 BOTTLE (11822-7891-9) 2020-06-010000-00-00NoNoCurrent