Package 0406-1850-01

{"route": ["ORAL"], "spl_id": "8ba92af8-0db9-4347-95c3-bd06680fc85f", "openfda": {"upc": ["0304061840019", "0304061810012", "0304061830010", "0304061860017", "0304061820011", "0304061850018"], "unii": ["4B3SC438HI"], "rxcui": ["1806181", "1806187", "1806189", "1806191", "1806193", "1806197"], "spl_set_id": ["9e11e093-4ff3-4bed-8fe9-3ee460b47303"], "manufacturer_name": ["SpecGx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0406-1850-01)", "package_ndc": "0406-1850-01", "marketing_start_date": "20150929"}], "brand_name": "Methylphenidate Hydrochloride Extended-Release", "product_id": "0406-1850_8ba92af8-0db9-4347-95c3-bd06680fc85f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "0406-1850", "dea_schedule": "CII", "generic_name": "methylphenidate hydrochloride", "labeler_name": "SpecGx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methylphenidate Hydrochloride", "brand_name_suffix": "Extended-Release", "active_ingredients": [{"name": "METHYLPHENIDATE HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203583", "marketing_category": "ANDA", "marketing_start_date": "20150929", "listing_expiration_date": "20261231"}