Package 71205-565-30

{"route": ["ORAL"], "spl_id": "64c33202-1fb1-4e0a-ae72-146375fa81aa", "openfda": {"upc": ["0371205565602"], "unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["909204fc-ff55-43d9-b9ee-e607ef60965e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-30)", "package_ndc": "71205-565-30", "marketing_start_date": "20210511"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-60)", "package_ndc": "71205-565-60", "marketing_start_date": "20210511"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-565-90)", "package_ndc": "71205-565-90", "marketing_start_date": "20210511"}], "brand_name": "bupropion", "product_id": "71205-565_64c33202-1fb1-4e0a-ae72-146375fa81aa", "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": "71205-565", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA202304", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}