Package 77771-144-05

{"route": ["ORAL"], "spl_id": "3bf617e4-22ef-4237-b80b-24c4c1b1bfda", "openfda": {"upc": ["0377771145903", "0377771145057", "0377771145309", "0377771144906", "0377771144302", "0377771144050"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541", "993557"], "spl_set_id": ["16a788ff-8bd5-4f70-a3fd-a89db019e435"], "manufacturer_name": ["RADHA PHARMACEUTICALS, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-05)", "package_ndc": "77771-144-05", "marketing_start_date": "20221026"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-30)", "package_ndc": "77771-144-30", "marketing_start_date": "20221026"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (77771-144-90)", "package_ndc": "77771-144-90", "marketing_start_date": "20221026"}], "brand_name": "Bupropion Hydrochloride (XL)", "product_id": "77771-144_3bf617e4-22ef-4237-b80b-24c4c1b1bfda", "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": "77771-144", "generic_name": "bupropion hydrochloride", "labeler_name": "RADHA 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": "20221026", "listing_expiration_date": "20271231"}