Package 69452-447-22

Brand: dual action pain reliever

Generic: acetaminophen and ibuprofen
NDC Package

Package Facts

Identity

Package NDC 69452-447-22
Digits Only 6945244722
Product NDC 69452-447
Description

1 BOTTLE in 1 CARTON (69452-447-22) / 120 TABLET, FILM COATED in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-08-08
Brand dual action pain reliever
Generic acetaminophen and ibuprofen
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1f2f8673-7d51-14b0-e063-6394a90afc7f", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["1f2f8fcf-bf08-2a21-e063-6394a90a9e71"], "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": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (69452-447-22)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "69452-447-22", "marketing_start_date": "20240808"}], "brand_name": "dual action pain reliever", "product_id": "69452-447_1f2f8673-7d51-14b0-e063-6394a90afc7f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69452-447", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dual action pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216999", "marketing_category": "ANDA", "marketing_start_date": "20240808", "listing_expiration_date": "20261231"}