Package 80425-0300-3

{"route": ["ORAL"], "spl_id": "2a9bf621-afbc-7627-e063-6294a90a77a9", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["f8af7829-8b61-6785-e053-6294a90af052"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-1)", "package_ndc": "80425-0300-1", "marketing_start_date": "20230406"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-2)", "package_ndc": "80425-0300-2", "marketing_start_date": "20230406"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0300-3)", "package_ndc": "80425-0300-3", "marketing_start_date": "20230406"}], "brand_name": "Bupropion hydrochloride", "product_id": "80425-0300_2a9bf621-afbc-7627-e063-6294a90a77a9", "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": "80425-0300", "generic_name": "Bupropion hydrochloride", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA210497", "marketing_category": "ANDA", "marketing_start_date": "20230406", "listing_expiration_date": "20261231"}