Package 68071-4968-4
Brand: ibuprofen
Generic: ibuprofenPackage Facts
Identity
Package NDC
68071-4968-4
Digits Only
6807149684
Product NDC
68071-4968
Description
40 TABLET, FILM COATED in 1 BOTTLE (68071-4968-4)
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": "47ad6d70-f32d-e896-e063-6294a90a0bbe", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071496833"], "unii": ["WK2XYI10QM"], "rxcui": ["197806"], "spl_set_id": ["8dba0ed8-feef-23a5-e053-2995a90aaff8"], "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": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4968-3)", "package_ndc": "68071-4968-3", "marketing_start_date": "20190715"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68071-4968-4)", "package_ndc": "68071-4968-4", "marketing_start_date": "20190715"}, {"sample": false, "description": "50 TABLET, FILM COATED in 1 BOTTLE (68071-4968-5)", "package_ndc": "68071-4968-5", "marketing_start_date": "20240910"}], "brand_name": "Ibuprofen", "product_id": "68071-4968_47ad6d70-f32d-e896-e063-6294a90a0bbe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-4968", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ibuprofen", "active_ingredients": [{"name": "IBUPROFEN", "strength": "600 mg/1"}], "application_number": "ANDA078329", "marketing_category": "ANDA", "marketing_start_date": "20140401", "listing_expiration_date": "20271231"}