Package 11822-5777-1
Brand: dual action
Generic: acetaminophen, ibuprofenPackage Facts
Identity
Package NDC
11822-5777-1
Digits Only
1182257771
Product NDC
11822-5777
Description
1 BOTTLE in 1 CARTON (11822-5777-1) / 72 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
dual action
Generic
acetaminophen, ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1655cbe6-86f3-4c51-afa9-936ef63f1195", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["54b08d24-d5e9-4111-9d97-329896e8309d"], "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": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-5777-0) / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-5777-0", "marketing_start_date": "20230524"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-5777-1) / 72 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-5777-1", "marketing_start_date": "20230524"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-5777-2) / 18 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-5777-2", "marketing_start_date": "20230524"}], "brand_name": "dual action", "product_id": "11822-5777_1655cbe6-86f3-4c51-afa9-936ef63f1195", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "11822-5777", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dual action", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA214836", "marketing_category": "ANDA", "marketing_start_date": "20230524", "listing_expiration_date": "20261231"}