FDA.reportPublic FDA data

IBUPROFEN

Product NDC
11673-991
11-digit product format
116730991
Labeler code
11673
Product ID
11673-991_0e071c42-0f7e-586e-e063-6394a90a9533
Type
HUMAN OTC DRUG
Nonproprietary name
IBUPROFEN
Dosage form
TABLET, COATED
Route
ORAL
Labeler
TARGET CORPORATION
Application
ANDA091239
Marketing category
ANDA
Marketing start
2020-02-04
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
11673-991-01IBUPROFEN100 in 1 BOTTLETABLET, COATED1008
11673-991-05IBUPROFEN50 in 1 BOTTLETABLET, COATED508
11673-991-20IBUPROFEN200 in 1 BOTTLETABLET, COATED2008
11673-991-50IBUPROFEN500 in 1 BOTTLETABLET, COATED5008
11673-991-88IBUPROFEN1000 in 1 BOTTLETABLET, COATED10008

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-991IBUPROFEN TABLET, COATED [TARGET CORPORATION]8Current NDC, Legacy NDC, 5 package rows20240104_8e86ae68-7687-79d6-e053-2995a90ac274.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
310965ibuprofen 200 MG Oral TabletPSN8e86ae68-7687-79d6-e053-2995a90ac2748
310965ibuprofen 200 MG Oral TabletSCD8e86ae68-7687-79d6-e053-2995a90ac2748
310965ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral TabletSY8e86ae68-7687-79d6-e053-2995a90ac2748

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
11673-991-0111673099101100 TABLET, COATED in 1 BOTTLE (11673-991-01) 2020-02-040000-00-00NoNoCurrent
11673-991-051167309910550 TABLET, COATED in 1 BOTTLE (11673-991-05) 2020-02-040000-00-00NoNoCurrent
11673-991-2011673099120200 TABLET, COATED in 1 BOTTLE (11673-991-20) 2020-02-040000-00-00NoNoCurrent
11673-991-5011673099150500 TABLET, COATED in 1 BOTTLE (11673-991-50) 2020-02-040000-00-00NoNoCurrent
11673-991-88116730991881000 TABLET, COATED in 1 BOTTLE (11673-991-88) 2020-02-040000-00-00NoNoCurrent