Package 71205-968-90

{"route": ["ORAL"], "spl_id": "f2be86a1-5401-4b68-a675-95b44c43a5f6", "openfda": {"upc": ["0371205967307"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["2af578d8-a7f8-4da3-b126-390a0e950fad"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-30)", "package_ndc": "71205-968-30", "marketing_start_date": "20200609"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-55)", "package_ndc": "71205-968-55", "marketing_start_date": "20200609"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71205-968-90)", "package_ndc": "71205-968-90", "marketing_start_date": "20200609"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "71205-968_f2be86a1-5401-4b68-a675-95b44c43a5f6", "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": "71205-968", "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": "ANDA210081", "marketing_category": "ANDA", "marketing_start_date": "20180830", "listing_expiration_date": "20261231"}