Package 82804-080-90

{"route": ["ORAL"], "spl_id": "dfd5f264-d4fd-4441-88b1-48086c7c0616", "openfda": {"upc": ["0382804080908"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["dfd5f264-d4fd-4441-88b1-48086c7c0616"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-30)", "package_ndc": "82804-080-30", "marketing_start_date": "20240305"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-60)", "package_ndc": "82804-080-60", "marketing_start_date": "20240305"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-080-90)", "package_ndc": "82804-080-90", "marketing_start_date": "20240305"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "82804-080_dfd5f264-d4fd-4441-88b1-48086c7c0616", "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": "82804-080", "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": "150 mg/1"}], "application_number": "ANDA210015", "marketing_category": "ANDA", "marketing_start_date": "20230430", "listing_expiration_date": "20261231"}