Package 50090-7113-0

{"route": ["ORAL"], "spl_id": "85ec5376-b7ef-4a0b-aa86-6918c483c520", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["6537007e-92c2-43ad-8387-5194cd2aff4c"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-0)", "package_ndc": "50090-7113-0", "marketing_start_date": "20240311"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-1)", "package_ndc": "50090-7113-1", "marketing_start_date": "20240311"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-7113-2)", "package_ndc": "50090-7113-2", "marketing_start_date": "20240311"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "50090-7113_85ec5376-b7ef-4a0b-aa86-6918c483c520", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-7113", "generic_name": "bupropion hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20230430", "listing_expiration_date": "20261231"}