Package 67877-655-01

{"route": ["ORAL"], "spl_id": "d87ba2c9-5dd1-4038-8149-7ef46c421422", "openfda": {"unii": ["1678OK0E08"], "rxcui": ["899518", "899548", "899557"], "spl_set_id": ["830df993-db01-40df-beef-90af6b86f561"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-655-01)", "package_ndc": "67877-655-01", "marketing_start_date": "20190721"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (67877-655-05)", "package_ndc": "67877-655-05", "marketing_start_date": "20190721"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (67877-655-30)", "package_ndc": "67877-655-30", "marketing_start_date": "20190721"}], "brand_name": "Dexmethylphenidate Hydrochloride", "product_id": "67877-655_d87ba2c9-5dd1-4038-8149-7ef46c421422", "dosage_form": "TABLET", "pharm_class": ["Central Nervous System Stimulant [EPC]", "Central Nervous System Stimulation [PE]"], "product_ndc": "67877-655", "dea_schedule": "CII", "generic_name": "Dexmethylphenidate Hydrochloride", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexmethylphenidate Hydrochloride", "active_ingredients": [{"name": "DEXMETHYLPHENIDATE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA212631", "marketing_category": "ANDA", "marketing_start_date": "20190721", "listing_expiration_date": "20261231"}