Package 51660-493-41

{"route": ["ORAL"], "spl_id": "f197efd7-d871-49e6-9984-51628bab7e8d", "openfda": {"nui": ["N0000000160", "M0001335", "N0000175722"], "unii": ["WK2XYI10QM", "6V9V2RYJ8N"], "rxcui": ["1299021"], "spl_set_id": ["cb7fb0d3-adf6-4c14-ac61-103dc869ebf2"], "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": ["Ohm Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "40 TABLET, SUGAR COATED in 1 BLISTER PACK (51660-493-41)", "package_ndc": "51660-493-41", "marketing_start_date": "20011013"}], "brand_name": "Ibuprofen and Pseudoephedrine hydrochloride", "product_id": "51660-493_f197efd7-d871-49e6-9984-51628bab7e8d", "dosage_form": "TABLET, SUGAR COATED", "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": "51660-493", "generic_name": "ibuprofen and pseudoephedrine hydrochloride", "labeler_name": "Ohm Laboratories Inc.", "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": "20011013", "listing_expiration_date": "20261231"}