Package 72189-539-90

{"route": ["ORAL"], "spl_id": "19b02d9d-9104-0442-e063-6394a90a3154", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["129ce80c-0333-873e-e063-6394a90a33e0"], "manufacturer_name": ["Direct_RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-30)", "package_ndc": "72189-539-30", "marketing_start_date": "20240301"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-539-90)", "package_ndc": "72189-539-90", "marketing_start_date": "20240301"}], "brand_name": "Bupropion HCL ER (XL)", "product_id": "72189-539_19b02d9d-9104-0442-e063-6394a90a3154", "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": "72189-539", "generic_name": "Bupropion HCL ER (XL)", "labeler_name": "Direct_RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion HCL ER (XL)", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20240301", "listing_expiration_date": "20261231"}