up and up ibuprofen

Generic: ibuprofen

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up ibuprofen
Generic Name ibuprofen
Labeler target corporation
Dosage Form SUSPENSION
Routes
ORAL
Active Ingredients

ibuprofen 100 mg/5mL

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-685
Product ID 11673-685_99910ab1-7456-4e03-9dd5-ba30a3e762d6
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA074937
Listing Expiration 2026-12-31
Marketing Start 2009-07-10

Pharmacologic Class

Established (EPC)
nonsteroidal anti-inflammatory drug [epc]
Mechanism of Action
cyclooxygenase inhibitors [moa]
Chemical Structure
anti-inflammatory agents, non-steroidal [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 11673685
Hyphenated Format 11673-685

Supplemental Identifiers

RxCUI
197803
UNII
WK2XYI10QM
NUI
N0000000160 M0001335 N0000175722

Packaging Origin

Original Packager
true

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 ibuprofen (source: ndc)
Generic Name ibuprofen (source: ndc)
Application Number ANDA074937 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/5mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (11673-685-26) / 118 mL in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-685-34) / 237 mL in 1 BOTTLE
source: ndc

Packages (2)

11673-685-26 1 BOTTLE in 1 CARTON (11673-685-26) / 118 mL in 1 BOTTLE 11673-685-34 1 BOTTLE in 1 CARTON (11673-685-34) / 237 mL in 1 BOTTLE

Ingredients (1)

ibuprofen (100 mg/5mL)

Linked Drug Pages (1)

up and up ibuprofen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "99910ab1-7456-4e03-9dd5-ba30a3e762d6", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197803"], "spl_set_id": ["6e0330ac-a111-4574-9197-d7aab33b8608"], "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 (11673-685-26)  / 118 mL in 1 BOTTLE", "package_ndc": "11673-685-26", "marketing_start_date": "20090710"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-685-34)  / 237 mL in 1 BOTTLE", "package_ndc": "11673-685-34", "marketing_start_date": "20110312"}], "brand_name": "up and up ibuprofen", "product_id": "11673-685_99910ab1-7456-4e03-9dd5-ba30a3e762d6", "dosage_form": "SUSPENSION", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11673-685", "generic_name": "Ibuprofen", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "up and up ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "100 mg/5mL"}], "application_number": "ANDA074937", "marketing_category": "ANDA", "marketing_start_date": "20090710", "listing_expiration_date": "20261231"}