Package 70000-0602-1

{"route": ["ORAL"], "spl_id": "b5d6426e-cfcc-40c9-b289-c2365eaf0fbb", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM", "6V9V2RYJ8N"], "rxcui": ["1299021"], "spl_set_id": ["2cccc119-8eea-4280-9ad9-ec29caf26940"], "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": ["CARDINAL HEALTH 110, LLC DBA LEADER"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET in 1 BLISTER PACK (70000-0602-1)", "package_ndc": "70000-0602-1", "marketing_start_date": "20220523"}], "brand_name": "IBUPROFEN and PSEUDOEPHEDRINE HYDROCHLORIDE", "product_id": "70000-0602_b5d6426e-cfcc-40c9-b289-c2365eaf0fbb", "dosage_form": "TABLET", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Anti-Inflammatory Agents", "Non-Steroidal [CS]", "Cyclooxygenase Inhibitors [MoA]", "Nonsteroidal Anti-inflammatory Drug [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "70000-0602", "generic_name": "IBUPROFEN and PSEUDOEPHEDRINE HYDROCHLORIDE", "labeler_name": "CARDINAL HEALTH 110, LLC DBA LEADER", "product_type": "HUMAN OTC DRUG", "brand_name_base": "IBUPROFEN and PSEUDOEPHEDRINE HYDROCHLORIDE", "active_ingredients": [{"name": "IBUPROFEN", "strength": "200 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA074567", "marketing_category": "ANDA", "marketing_start_date": "20220523", "listing_expiration_date": "20261231"}