Package 0406-8330-01

{"route": ["ORAL"], "spl_id": "6873cac9-e7d5-4db2-851d-528268b483e9", "openfda": {"upc": ["0304068320019"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["533034fd-c8e7-495b-8874-0db41bd1e65a"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-8330-01)", "package_ndc": "0406-8330-01", "marketing_start_date": "20030731"}, {"sample": false, "description": "1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8330-23)", "package_ndc": "0406-8330-23", "marketing_start_date": "20030731"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0406-8330-62)", "package_ndc": "0406-8330-62", "marketing_start_date": "20030731"}], "brand_name": "MORPHINE SULFATE", "product_id": "0406-8330_6873cac9-e7d5-4db2-851d-528268b483e9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "0406-8330", "dea_schedule": "CII", "generic_name": "MORPHINE SULFATE", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MORPHINE SULFATE", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "30 mg/1"}], "application_number": "ANDA076412", "marketing_category": "ANDA", "marketing_start_date": "20030731", "listing_expiration_date": "20261231"}