Package 63304-497-10

{"route": ["ORAL"], "spl_id": "4f875c7a-4454-45a2-bf55-fcc2932c51db", "openfda": {"upc": ["0363304497014"], "unii": ["362O9ITL9D", "NO70W886KK"], "rxcui": ["856999"], "spl_set_id": ["6e153073-ca78-481e-9e9c-0365ee3f3d59"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63304-497-01)", "package_ndc": "63304-497-01", "marketing_start_date": "20180731"}, {"sample": false, "description": "10 TABLET in 1 BOTTLE (63304-497-03)", "package_ndc": "63304-497-03", "marketing_start_date": "20180731"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (63304-497-05)", "package_ndc": "63304-497-05", "marketing_start_date": "20180731"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (63304-497-10)", "package_ndc": "63304-497-10", "marketing_start_date": "20180731"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (63304-497-69)  / 1 TABLET in 1 BLISTER PACK (63304-497-11)", "package_ndc": "63304-497-69", "marketing_start_date": "20180731"}], "brand_name": "Hydrocodone Bitartrate and Acetaminophen", "product_id": "63304-497_4f875c7a-4454-45a2-bf55-fcc2932c51db", "dosage_form": "TABLET", "pharm_class": ["Opioid Agonist [EPC]", "Opioid Agonists [MoA]"], "product_ndc": "63304-497", "dea_schedule": "CII", "generic_name": "Hydrocodone Bitartrate and Acetaminophen", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrocodone Bitartrate and Acetaminophen", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "325 mg/1"}, {"name": "HYDROCODONE BITARTRATE", "strength": "10 mg/1"}], "application_number": "ANDA040826", "marketing_category": "ANDA", "marketing_start_date": "20180731", "listing_expiration_date": "20261231"}