Package 63304-453-05

{"route": ["ORAL"], "spl_id": "39a0166a-c2ca-47bf-8654-85e0a431b9a0", "openfda": {"upc": ["0363304453010", "0363304758016", "0363304452013", "0363304450019", "0363304451016"], "unii": ["X3P646A2J0"], "rxcui": ["891874", "891881", "891888", "891893", "892646"], "spl_set_id": ["736c9b80-682c-4cda-bf18-61b18de0bd39"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-453-01)", "package_ndc": "63304-453-01", "marketing_start_date": "20120511"}, {"sample": false, "description": "10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-453-03)", "package_ndc": "63304-453-03", "marketing_start_date": "20120511"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-453-05)", "package_ndc": "63304-453-05", "marketing_start_date": "20120511"}], "brand_name": "Morphine sulfate", "product_id": "63304-453_39a0166a-c2ca-47bf-8654-85e0a431b9a0", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "63304-453", "dea_schedule": "CII", "generic_name": "morphine sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Morphine sulfate", "active_ingredients": [{"name": "MORPHINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA078761", "marketing_category": "ANDA", "marketing_start_date": "20120511", "listing_expiration_date": "20261231"}