Package 11673-685-34

Brand: up and up ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 11673-685-34
Digits Only 1167368534
Product NDC 11673-685
Description

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

Marketing

Marketing Status
Marketed Since 2011-03-12
Brand up and up ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

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"}