Up and Up childrens ibuprofen

Product NDC
11673-166
11-digit product format
116730166
Labeler code
11673
Product ID
11673-166_ab380f8c-73e9-429c-80d6-05929e72eae4
Type
HUMAN OTC DRUG
Nonproprietary name
Ibuprofen
Dosage form
SUSPENSION
Route
ORAL
Labeler
Target Corporation
Application
ANDA074937
Marketing category
ANDA
Marketing start
2009-06-12
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 childrens 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
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
874f4e63-49d2-5150-5d77-052172814ebdProduct name620230105
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
557673c2-8256-b351-e863-4ec71a5a64b0Product name220160714
dbc9a339-6215-4e94-9546-57a3b34902ceProduct name120160517
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
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
11673-166-26Up and Up childrens ibuprofen118 mL in 1 BOTTLESUSPENSION1188
11673-166-26Up and Up childrens ibuprofen1 in 1 CARTONSUSPENSION18
11673-166-28Up and Up childrens ibuprofen1 in 1 CARTONSUSPENSION18
11673-166-28Up and Up childrens ibuprofen148 mL in 1 BOTTLESUSPENSION1488
11673-166-34Up and Up childrens ibuprofen237 mL in 1 BOTTLESUSPENSION2378
11673-166-34Up and Up childrens ibuprofen1 in 1 CARTONSUSPENSION18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
11673-166UP AND UP CHILDRENS IBUPROFEN (IBUPROFEN) SUSPENSION [TARGET CORPORATION]8Current NDC, Legacy NDC, 6 package rows20250514_28911692-882b-4e30-ba1d-5c10f847be80.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197803ibuprofen 100 MG in 5 mL Oral SuspensionPSN28911692-882b-4e30-ba1d-5c10f847be808
197803ibuprofen 20 MG/ML Oral SuspensionSCD28911692-882b-4e30-ba1d-5c10f847be808
197803ibuprofen 100 MG per 5 ML Oral SuspensionSY28911692-882b-4e30-ba1d-5c10f847be808
197803ibuprofen 200 MG per 10 ML Oral SuspensionSY28911692-882b-4e30-ba1d-5c10f847be808

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11673-166-26116730166261 BOTTLE in 1 CARTON (11673-166-26) > 118 mL in 1 BOTTLE1 bottle2009-06-120000-00-00NoNoCurrent
11673-166-28116730166281 in 1 CARTONHistorical
11673-166-34116730166341 BOTTLE in 1 CARTON (11673-166-34) / 237 mL in 1 BOTTLE1 bottle2013-02-190000-00-00NoNoCurrent