FDA.reportPublic FDA data

up and up ibuprofen

Product NDC
11673-685
11-digit product format
116730685
Labeler code
11673
Product ID
11673-685_99910ab1-7456-4e03-9dd5-ba30a3e762d6
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Target Corporation
Application
ANDA074937
Marketing category
ANDA
Marketing start
2009-07-10
Substance
IBUPROFEN
Active strength
100 mg/5mL
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
up and up ibuprofen
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
IBUPROFEN100 mg/5mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiWK2XYI10QM
Rxcui197803

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
11673-685-26up and up ibuprofen118 mL in 1 BOTTLESUSPENSION1186
11673-685-26up and up ibuprofen1 in 1 CARTONSUSPENSION16
11673-685-28up and up ibuprofen1 in 1 CARTONSUSPENSION16
11673-685-28up and up ibuprofen148 mL in 1 BOTTLESUSPENSION1486
11673-685-34up and up ibuprofen237 mL in 1 BOTTLESUSPENSION2376
11673-685-34up and up ibuprofen1 in 1 CARTONSUSPENSION16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-685UP AND UP IBUPROFEN (IBUPROFEN) SUSPENSION [TARGET CORPORATION]6Current NDC, Legacy NDC, 6 package rows20250508_6e0330ac-a111-4574-9197-d7aab33b8608.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197803ibuprofen 100 MG in 5 mL Oral SuspensionPSN6e0330ac-a111-4574-9197-d7aab33b86086
197803ibuprofen 20 MG/ML Oral SuspensionSCD6e0330ac-a111-4574-9197-d7aab33b86086
197803ibuprofen 100 MG per 5 ML Oral SuspensionSY6e0330ac-a111-4574-9197-d7aab33b86086
197803ibuprofen 200 MG per 10 ML Oral SuspensionSY6e0330ac-a111-4574-9197-d7aab33b86086

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-685-26116730685261 BOTTLE in 1 CARTON (11673-685-26) / 118 mL in 1 BOTTLE1 bottle2009-07-100000-00-00NoNoCurrent
11673-685-28116730685281 in 1 CARTONHistorical
11673-685-34116730685341 BOTTLE in 1 CARTON (11673-685-34) / 237 mL in 1 BOTTLE1 bottle2011-03-120000-00-00NoNoCurrent