Package 68071-3053-6
Brand: ibu
Generic: ibuprofenPackage Facts
Identity
Package NDC
68071-3053-6
Digits Only
6807130536
Product NDC
68071-3053
Description
60 TABLET in 1 BOTTLE (68071-3053-6)
Marketing
Marketing Status
Brand
ibu
Generic
ibuprofen
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d8e3521-5b6d-3418-e063-6294a90a9c41", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071305333"], "unii": ["WK2XYI10QM"], "rxcui": ["197807", "206917"], "spl_set_id": ["678e2d16-33f3-67a7-e053-2991aa0a1132"], "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": "12 TABLET in 1 BOTTLE (68071-3053-0)", "package_ndc": "68071-3053-0", "marketing_start_date": "20180316"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (68071-3053-1)", "package_ndc": "68071-3053-1", "marketing_start_date": "20180316"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (68071-3053-2)", "package_ndc": "68071-3053-2", "marketing_start_date": "20180316"}, {"sample": false, "description": "40 TABLET in 1 BOTTLE (68071-3053-4)", "package_ndc": "68071-3053-4", "marketing_start_date": "20180316"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3053-6)", "package_ndc": "68071-3053-6", "marketing_start_date": "20180316"}], "brand_name": "IBU", "product_id": "68071-3053_1d8e3521-5b6d-3418-e063-6294a90a9c41", "dosage_form": "TABLET", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3053", "generic_name": "Ibuprofen", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBU", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA075682", "marketing_category": "ANDA", "marketing_start_date": "20081120", "listing_expiration_date": "20261231"}