Package 43598-579-30

{"route": ["BUCCAL", "SUBLINGUAL"], "spl_id": "94051f2a-cce3-5dcf-8960-1d36168d77c0", "openfda": {"nui": ["N0000175691", "N0000000154"], "upc": ["0343598579016", "0343598582016"], "unii": ["36B82AMQ7N", "56W8MW3EN1"], "rxcui": ["1010600", "1010604"], "spl_set_id": ["718756d7-0131-b173-6c45-5ee039b311b0"], "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 (43598-579-30)  / 1 FILM, SOLUBLE in 1 POUCH (43598-579-01)", "package_ndc": "43598-579-30", "marketing_start_date": "20180614"}], "brand_name": "Buprenorphine and Naloxone", "product_id": "43598-579_94051f2a-cce3-5dcf-8960-1d36168d77c0", "dosage_form": "FILM, SOLUBLE", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]", "Partial Opioid Agonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "43598-579", "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": "2 mg/1"}, {"name": "NALOXONE", "strength": ".5 mg/1"}], "application_number": "ANDA205299", "marketing_category": "ANDA", "marketing_start_date": "20180614", "listing_expiration_date": "20271231"}