Package 50090-1869-0

{"route": ["ORAL"], "spl_id": "aa89dc60-57fd-465a-9c47-8aa53221bd91", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["78ef709a-f835-4b03-92dd-16a4c82af0c1"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-1869-0)", "package_ndc": "50090-1869-0", "marketing_start_date": "20150610"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-1869-3)", "package_ndc": "50090-1869-3", "marketing_start_date": "20150610"}], "brand_name": "Bupropion Hydrochloride", "product_id": "50090-1869_aa89dc60-57fd-465a-9c47-8aa53221bd91", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-1869", "generic_name": "Bupropion Hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}