Package 71205-357-24
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
71205-357-24
Digits Only
7120535724
Product NDC
71205-357
Description
24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)
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": "c18cb763-af0c-4cc2-b7df-520835c91884", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0371205357603"], "unii": ["WK2XYI10QM"], "rxcui": ["310965"], "spl_set_id": ["798d33b0-5d7a-4445-8a51-2a3d336f744a"], "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": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (71205-357-06)", "package_ndc": "71205-357-06", "marketing_start_date": "20191112"}, {"sample": false, "description": "24 TABLET, FILM COATED in 1 BOTTLE (71205-357-24)", "package_ndc": "71205-357-24", "marketing_start_date": "20210826"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-357-30)", "package_ndc": "71205-357-30", "marketing_start_date": "20191112"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (71205-357-50)", "package_ndc": "71205-357-50", "marketing_start_date": "20191112"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-357-60)", "package_ndc": "71205-357-60", "marketing_start_date": "20191112"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-357-90)", "package_ndc": "71205-357-90", "marketing_start_date": "20191112"}], "brand_name": "ibuprofen", "product_id": "71205-357_c18cb763-af0c-4cc2-b7df-520835c91884", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "71205-357", "generic_name": "Ibuprofen", "labeler_name": "Proficient Rx LP", "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": "20180920", "listing_expiration_date": "20261231"}