Package 47335-860-08

{"route": ["ORAL"], "spl_id": "a994e116-d201-47f9-baaf-dd76a84eba7e", "openfda": {"upc": ["0347335861839", "0347335860832", "0347335859836"], "unii": ["9N7R477WCK"], "rxcui": ["833709", "833711", "833713"], "spl_set_id": ["004de5a4-80f8-4040-a6ea-be5e99352a36"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-08)", "package_ndc": "47335-860-08", "marketing_start_date": "20111212"}, {"sample": false, "description": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-18)", "package_ndc": "47335-860-18", "marketing_start_date": "20111212"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-83)", "package_ndc": "47335-860-83", "marketing_start_date": "20111212"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-88)", "package_ndc": "47335-860-88", "marketing_start_date": "20111212"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "47335-860_a994e116-d201-47f9-baaf-dd76a84eba7e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "47335-860", "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": "200 mg/1"}], "application_number": "ANDA201384", "marketing_category": "ANDA", "marketing_start_date": "20111212", "listing_expiration_date": "20261231"}