Package 82804-013-90

{"route": ["ORAL"], "spl_id": "80f4a4ef-8190-458d-af2e-5daaf32abc01", "openfda": {"upc": ["0382804013302"], "unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["80f4a4ef-8190-458d-af2e-5daaf32abc01"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-30)", "package_ndc": "82804-013-30", "marketing_start_date": "20230921"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-60)", "package_ndc": "82804-013-60", "marketing_start_date": "20230921"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-013-90)", "package_ndc": "82804-013-90", "marketing_start_date": "20230921"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "82804-013_80f4a4ef-8190-458d-af2e-5daaf32abc01", "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": "82804-013", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "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": "ANDA206556", "marketing_category": "ANDA", "marketing_start_date": "20160829", "listing_expiration_date": "20261231"}