FDA.reportPublic FDA data

IBUPROFEN

Product NDC
11822-7892
11-digit product format
118227892
Labeler code
11822
Product ID
11822-7892_cf2caf6f-2192-2428-e053-2995a90aae6d
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
11822-7892-0IBUPROFEN24 in 1 BOTTLETABLET, COATED242
11822-7892-2IBUPROFEN50 in 1 BOTTLETABLET, COATED502
11822-7892-5IBUPROFEN100 in 1 BOTTLETABLET, COATED1002
11822-7892-7IBUPROFEN200 in 1 BOTTLETABLET, COATED2002
11822-7892-9IBUPROFEN500 in 1 BOTTLETABLET, COATED5002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11822-7892IBUPROFEN TABLET, COATED [RITE AID CORPORATION]2Current NDC, Legacy NDC, 5 package rows20211031_a7abac4c-7695-cfe8-e053-2a95a90ac1cd.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSNa7abac4c-7695-cfe8-e053-2a95a90ac1cd2
310965ibuprofen 200 MG Oral TabletSCDa7abac4c-7695-cfe8-e053-2a95a90ac1cd2
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSYa7abac4c-7695-cfe8-e053-2a95a90ac1cd2

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11822-7892-01182278920024 TABLET, COATED in 1 BOTTLE (11822-7892-0) 2020-06-010000-00-00NoNoCurrent
11822-7892-21182278920250 TABLET, COATED in 1 BOTTLE (11822-7892-2) 2020-06-010000-00-00NoNoCurrent
11822-7892-511822789205100 TABLET, COATED in 1 BOTTLE (11822-7892-5) 2020-06-010000-00-00NoNoCurrent
11822-7892-711822789207200 TABLET, COATED in 1 BOTTLE (11822-7892-7) 2020-06-010000-00-00NoNoCurrent
11822-7892-911822789209500 TABLET, COATED in 1 BOTTLE (11822-7892-9) 2020-06-010000-00-00NoNoCurrent