Package 80425-0468-1

{"route": ["ORAL"], "spl_id": "2aabf642-2904-a735-e063-6394a90a83b5", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["2aabf040-16a6-b772-e063-6294a90afd70"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-1)", "package_ndc": "80425-0468-1", "marketing_start_date": "20250101"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-2)", "package_ndc": "80425-0468-2", "marketing_start_date": "20250101"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0468-3)", "package_ndc": "80425-0468-3", "marketing_start_date": "20250101"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "80425-0468_2aabf642-2904-a735-e063-6394a90a83b5", "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": "80425-0468", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "XL", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA207224", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}