Package 68071-3362-9

{"route": ["ORAL"], "spl_id": "1ce905e8-9477-0b57-e063-6394a90ab525", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "upc": ["0368071336238"], "unii": ["WK2XYI10QM"], "rxcui": ["197807"], "spl_set_id": ["553c8cfa-cf0f-0b1f-e054-00144ff88e88"], "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, FILM COATED in 1 BOTTLE (68071-3362-0)", "package_ndc": "68071-3362-0", "marketing_start_date": "20170726"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1)", "package_ndc": "68071-3362-1", "marketing_start_date": "20170726"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68071-3362-2)", "package_ndc": "68071-3362-2", "marketing_start_date": "20170726"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3362-3)", "package_ndc": "68071-3362-3", "marketing_start_date": "20170726"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE (68071-3362-4)", "package_ndc": "68071-3362-4", "marketing_start_date": "20170726"}, {"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (68071-3362-5)", "package_ndc": "68071-3362-5", "marketing_start_date": "20170726"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-3362-6)", "package_ndc": "68071-3362-6", "marketing_start_date": "20170726"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-3362-9)", "package_ndc": "68071-3362-9", "marketing_start_date": "20170726"}], "brand_name": "IBUPROFEN", "product_id": "68071-3362_1ce905e8-9477-0b57-e063-6394a90ab525", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]"], "product_ndc": "68071-3362", "generic_name": "IBUPROFEN", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IBUPROFEN", "active_ingredients": [{"name": "IBUPROFEN", "strength": "800 mg/1"}], "application_number": "ANDA090796", "marketing_category": "ANDA", "marketing_start_date": "20151230", "listing_expiration_date": "20261231"}