Package 54123-986-30

{"route": ["SUBLINGUAL"], "spl_id": "8c67e97f-118f-4226-972a-a9031ef6f5ce", "openfda": {"unii": ["56W8MW3EN1", "F850569PQR"], "rxcui": ["1431076", "1431083", "1431102", "1431104", "1597568", "1597570", "1597573", "1597575", "1666338", "1666385", "1864412", "1864414"], "spl_set_id": ["5f5cfcfe-d52b-49e6-8fe4-550477332dd2"], "manufacturer_name": ["Orexo US, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 CARTON (54123-986-30)  / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK", "package_ndc": "54123-986-30", "marketing_start_date": "20141211"}], "brand_name": "Zubsolv", "product_id": "54123-986_8c67e97f-118f-4226-972a-a9031ef6f5ce", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "54123-986", "dea_schedule": "CIII", "generic_name": "buprenorphine hydrochloride and naloxone hydrochloride", "labeler_name": "Orexo US, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zubsolv", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "8.6 mg/1"}, {"name": "NALOXONE HYDROCHLORIDE", "strength": "2.1 mg/1"}], "application_number": "NDA204242", "marketing_category": "NDA", "marketing_start_date": "20141211", "listing_expiration_date": "20261231"}