Package 68788-4039-8
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
68788-4039-8
Digits Only
6878840398
Product NDC
68788-4039
Description
28 TABLET, FILM COATED in 1 BOTTLE (68788-4039-8)
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": "a85080d7-50b4-461b-9d77-d6fbab971c03", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM"], "rxcui": ["197805"], "spl_set_id": ["a85080d7-50b4-461b-9d77-d6fbab971c03"], "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": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68788-4039-1)", "package_ndc": "68788-4039-1", "marketing_start_date": "20251013"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-4039-2)", "package_ndc": "68788-4039-2", "marketing_start_date": "20251013"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-4039-3)", "package_ndc": "68788-4039-3", "marketing_start_date": "20251013"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (68788-4039-5)", "package_ndc": "68788-4039-5", "marketing_start_date": "20251013"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-4039-6)", "package_ndc": "68788-4039-6", "marketing_start_date": "20251013"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (68788-4039-8)", "package_ndc": "68788-4039-8", "marketing_start_date": "20251013"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-4039-9)", "package_ndc": "68788-4039-9", "marketing_start_date": "20251013"}], "brand_name": "Ibuprofen", "product_id": "68788-4039_a85080d7-50b4-461b-9d77-d6fbab971c03", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68788-4039", "generic_name": "Ibuprofen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "400 mg/1"}], "application_number": "ANDA202413", "marketing_category": "ANDA", "marketing_start_date": "20251013", "listing_expiration_date": "20261231"}