Package 47335-537-18

{"route": ["ORAL"], "spl_id": "e080bc94-c122-41f3-8bda-0fb9318f8aa6", "openfda": {"upc": ["0347335533835", "0347335537833", "0347335531831"], "unii": ["9N7R477WCK"], "rxcui": ["1946525", "1946527", "1946529"], "spl_set_id": ["dc420d50-6192-482d-b3da-3be55870a79a"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-08)", "package_ndc": "47335-537-08", "marketing_start_date": "20111230"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-18)", "package_ndc": "47335-537-18", "marketing_start_date": "20111230"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-83)", "package_ndc": "47335-537-83", "marketing_start_date": "20111230"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-88)", "package_ndc": "47335-537-88", "marketing_start_date": "20111230"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "47335-537_e080bc94-c122-41f3-8bda-0fb9318f8aa6", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "47335-537", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA091607", "marketing_category": "ANDA", "marketing_start_date": "20111230", "listing_expiration_date": "20261231"}