Package 71205-550-90

{"route": ["ORAL"], "spl_id": "aa8b309e-c87e-45a7-81b0-e83412015a27", "openfda": {"upc": ["0371205550301"], "unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["1094ff8e-f5a5-4a72-8bf9-25e68f5c964a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-550-30)", "package_ndc": "71205-550-30", "marketing_start_date": "20210401"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-550-60)", "package_ndc": "71205-550-60", "marketing_start_date": "20210401"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-550-90)", "package_ndc": "71205-550-90", "marketing_start_date": "20210401"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "71205-550_aa8b309e-c87e-45a7-81b0-e83412015a27", "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": "71205-550", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20261231"}