Package 43598-580-30

{"route": ["BUCCAL", "SUBLINGUAL"], "spl_id": "af3c8314-5a38-2103-6ef8-94f179ffd541", "openfda": {"nui": ["N0000175691", "N0000000154"], "upc": ["0343598580012"], "unii": ["36B82AMQ7N", "56W8MW3EN1"], "rxcui": ["1307056", "1307061"], "spl_set_id": ["72dc1ec0-7c59-a587-4ffd-c40ef79e6fb2"], "pharm_class_epc": ["Opioid Antagonist [EPC]"], "pharm_class_moa": ["Opioid Antagonists [MoA]"], "manufacturer_name": ["Dr.Reddys Laboratories Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 POUCH in 1 CARTON (43598-580-30)  / 1 FILM, SOLUBLE in 1 POUCH (43598-580-01)", "package_ndc": "43598-580-30", "marketing_start_date": "20180614"}], "brand_name": "Buprenorphine and Naloxone", "product_id": "43598-580_af3c8314-5a38-2103-6ef8-94f179ffd541", "dosage_form": "FILM, SOLUBLE", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "43598-580", "dea_schedule": "CIII", "generic_name": "Buprenorphine and Naloxone", "labeler_name": "Dr.Reddys Laboratories Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Buprenorphine and Naloxone", "active_ingredients": [{"name": "BUPRENORPHINE HYDROCHLORIDE", "strength": "4 mg/1"}, {"name": "NALOXONE", "strength": "1 mg/1"}], "application_number": "ANDA205806", "marketing_category": "ANDA", "marketing_start_date": "20180614", "listing_expiration_date": "20271231"}