up and up childrens ibuprofen
Generic: ibuprofen
Labeler: target corporationDrug Facts
Product Profile
Brand Name
up and up childrens ibuprofen
Generic Name
ibuprofen
Labeler
target corporation
Dosage Form
SUSPENSION
Routes
Active Ingredients
ibuprofen 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
11673-166
Product ID
11673-166_ab380f8c-73e9-429c-80d6-05929e72eae4
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA074937
Listing Expiration
2026-12-31
Marketing Start
2009-06-12
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11673166
Hyphenated Format
11673-166
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
up and up childrens ibuprofen (source: ndc)
Generic Name
ibuprofen (source: ndc)
Application Number
ANDA074937 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/5mL
Packaging
- 1 BOTTLE in 1 CARTON (11673-166-34) / 237 mL in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ab380f8c-73e9-429c-80d6-05929e72eae4", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["28911692-882b-4e30-ba1d-5c10f847be80"], "pharm_class_cs": ["Anti-Inflammatory Agents, Non-Steroidal [CS]"], "pharm_class_epc": ["Nonsteroidal Anti-inflammatory Drug [EPC]"], "pharm_class_moa": ["Cyclooxygenase Inhibitors [MoA]"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-166-34) / 237 mL in 1 BOTTLE", "package_ndc": "11673-166-34", "marketing_start_date": "20130219"}], "brand_name": "Up and Up childrens ibuprofen", "product_id": "11673-166_ab380f8c-73e9-429c-80d6-05929e72eae4", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-166", "generic_name": "Ibuprofen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up childrens ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA074937", "marketing_category": "ANDA", "marketing_start_date": "20090612", "listing_expiration_date": "20261231"}