Package 59011-410-20

{"route": ["ORAL"], "spl_id": "fee11108-8569-42d8-9e41-e49906b7a0be", "openfda": {"unii": ["C1ENJ2TE6C"], "rxcui": ["1049504", "1049545", "1049565", "1049576", "1049586", "1049595", "1049601", "1860127", "1860129", "1860137", "1860148", "1860151", "1860154", "1860157"], "spl_set_id": ["bfdfe235-d717-4855-a3c8-a13d26dadede"], "manufacturer_name": ["Purdue Pharma LP"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59011-410-10)", "package_ndc": "59011-410-10", "marketing_start_date": "20100808"}, {"sample": false, "description": "2 BLISTER PACK in 1 CARTON (59011-410-20)  / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "59011-410-20", "marketing_start_date": "20100808"}], "brand_name": "OxyContin", "product_id": "59011-410_fee11108-8569-42d8-9e41-e49906b7a0be", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "59011-410", "dea_schedule": "CII", "generic_name": "oxycodone hydrochloride", "labeler_name": "Purdue Pharma LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OxyContin", "active_ingredients": [{"name": "OXYCODONE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA022272", "marketing_category": "NDA", "marketing_start_date": "20100808", "listing_expiration_date": "20271231"}