Package 69452-394-64
Brand: acetaminophen and ibuprofen
Generic: acetaminophen and ibuprofenPackage Facts
Identity
Package NDC
69452-394-64
Digits Only
6945239464
Product NDC
69452-394
Description
216 TABLET, FILM COATED in 1 BOTTLE (69452-394-64)
Marketing
Marketing Status
Brand
acetaminophen and ibuprofen
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": "45c4da17-7d0d-421b-e063-6294a90a6a2e", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["04ccc4b2-0cfd-3012-e063-6394a90afa79"], "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": "216 TABLET, FILM COATED in 1 BOTTLE (69452-394-64)", "package_ndc": "69452-394-64", "marketing_start_date": "20230908"}, {"sample": false, "description": "400 TABLET, FILM COATED in 1 BOTTLE (69452-394-81)", "package_ndc": "69452-394-81", "marketing_start_date": "20251205"}], "brand_name": "Acetaminophen and Ibuprofen", "product_id": "69452-394_45c4da17-7d0d-421b-e063-6294a90a6a2e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "69452-394", "generic_name": "Acetaminophen and Ibuprofen", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Acetaminophen and Ibuprofen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA216999", "marketing_category": "ANDA", "marketing_start_date": "20230908", "listing_expiration_date": "20261231"}