Package 83008-082-30

{"route": ["ORAL"], "spl_id": "2f1417b0-2b35-4e9c-a9c4-e17d3d51d8e7", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["57a9f4d3-0c41-4978-b81e-cf3059bc8c42"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83008-082-30)", "package_ndc": "83008-082-30", "marketing_end_date": "20261231", "marketing_start_date": "20240828"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "83008-082_2f1417b0-2b35-4e9c-a9c4-e17d3d51d8e7", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "83008-082", "generic_name": "bupropion hydrochloride", "labeler_name": "Quality Care Products, LLC", "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": "ANDA207479", "marketing_category": "ANDA", "marketing_end_date": "20261231", "marketing_start_date": "20240828"}