Package 0363-5220-16
Brand: dual pain reliever
Generic: acetaminophen, ibuprofenPackage Facts
Identity
Package NDC
0363-5220-16
Digits Only
0363522016
Product NDC
0363-5220
Description
1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE
Marketing
Marketing Status
Brand
dual pain reliever
Generic
acetaminophen, ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f64cb05e-be18-481e-894f-bdc0b8c2ef88", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["362O9ITL9D", "WK2XYI10QM"], "rxcui": ["2387532"], "spl_set_id": ["5cb3b0b4-5b47-4ed4-a5e3-f14dbbcb46df"], "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": ["Walgreen Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-01) / 216 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-01", "marketing_start_date": "20231211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-16) / 144 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-16", "marketing_start_date": "20231211"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-23) / 72 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-23", "marketing_start_date": "20230310"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0363-5220-68) / 36 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "0363-5220-68", "marketing_start_date": "20230310"}], "brand_name": "dual pain reliever", "product_id": "0363-5220_f64cb05e-be18-481e-894f-bdc0b8c2ef88", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "0363-5220", "generic_name": "Acetaminophen, Ibuprofen", "labeler_name": "Walgreen Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "dual pain reliever", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "250 mg/1"}, {"name": "IBUPROFEN", "strength": "125 mg/1"}], "application_number": "ANDA214836", "marketing_category": "ANDA", "marketing_start_date": "20230310", "listing_expiration_date": "20261231"}