Package 68071-3927-3

{"route": ["ORAL"], "spl_id": "459bd306-cf69-8de4-e063-6394a90ae48d", "openfda": {"upc": ["0368071392739"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["459bd1c9-d7a5-8bc9-e063-6394a90a8ecd"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68071-3927-3)", "package_ndc": "68071-3927-3", "marketing_start_date": "20251210"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "68071-3927_459bd306-cf69-8de4-e063-6394a90ae48d", "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": "68071-3927", "generic_name": "bupropion hydrochloride", "labeler_name": "NuCare Pharmaceuticals, Inc.", "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_start_date": "20170412", "listing_expiration_date": "20261231"}