Package 68016-645-12

Brand: ibuprofen

Generic: ibuprofen
NDC Package

Package Facts

Identity

Package NDC 68016-645-12
Digits Only 6801664512
Product NDC 68016-645
Description

1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC

Marketing

Marketing Status
Discontinued 2026-08-31
Brand ibuprofen
Generic ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d2415143-02bb-4721-9d15-68833cbc7efb", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0840986031502"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["409941dc-9fd3-4475-bc6c-defe3cfbc61a"], "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": ["Chain Drug Consortium"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-08)  / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-08", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-12)  / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-12", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}, {"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (68016-645-15)  / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC", "package_ndc": "68016-645-15", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}], "brand_name": "Ibuprofen", "product_id": "68016-645_d2415143-02bb-4721-9d15-68833cbc7efb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68016-645", "generic_name": "Ibuprofen", "labeler_name": "Chain Drug Consortium", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA075010", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "19880524"}