Package 56062-604-90
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
56062-604-90
Digits Only
5606260490
Product NDC
56062-604
Description
500 TABLET, FILM COATED in 1 BOTTLE (56062-604-90)
Marketing
Marketing Status
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": "42166a6e-a38b-446b-837e-3cf2e52a8a3d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["2dd98554-e434-4617-b789-6ecce7144988"], "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": ["Publix Super Markets Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-71) / 50 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-71", "marketing_start_date": "20021226"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-78) / 100 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-78", "marketing_start_date": "19880915"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (56062-604-85) / 250 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "56062-604-85", "marketing_start_date": "20000320"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (56062-604-90)", "package_ndc": "56062-604-90", "marketing_start_date": "20041021"}], "brand_name": "ibuprofen", "product_id": "56062-604_42166a6e-a38b-446b-837e-3cf2e52a8a3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "56062-604", "generic_name": "Ibuprofen", "labeler_name": "Publix Super Markets Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}], "application_number": "ANDA072096", "marketing_category": "ANDA", "marketing_start_date": "19880915", "listing_expiration_date": "20261231"}