Package 3215-6524-30

{"route": ["BUCCAL", "SUBLINGUAL"], "spl_id": "3afe7278-3008-3b01-e063-6294a90a88bf", "openfda": {"unii": ["56W8MW3EN1", "F850569PQR"], "rxcui": ["1010600", "1010604", "1307056", "1307061"], "spl_set_id": ["cb112448-49a1-4209-bcdb-7cfae6501f51"], "manufacturer_name": ["Aveva Drug Delivery Systems Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (3215-6524-30)  / 1 FILM in 1 POUCH (3215-6524-01)", "package_ndc": "3215-6524-30", "marketing_start_date": "20230829"}], "brand_name": "Buprenorphine and Naloxone", "product_id": "3215-6524_3afe7278-3008-3b01-e063-6294a90a88bf", "dosage_form": "FILM", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "3215-6524", "dea_schedule": "CIII", "generic_name": "buprenorphine and naloxone", "labeler_name": "Aveva Drug Delivery Systems Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine and Naloxone", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "12 mg/1"}, {"name": "NALOXONE HYDROCHLORIDE", "strength": "3 mg/1"}], "application_number": "ANDA212756", "marketing_category": "ANDA", "marketing_start_date": "20230829", "listing_expiration_date": "20261231"}