Package 71205-291-60

{"route": ["ORAL"], "spl_id": "ee865180-23ee-4b72-a56e-30db9551dddc", "openfda": {"upc": ["0371205291303"], "unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["5e568bb5-542a-4395-a21e-dc64281d694e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-30)", "package_ndc": "71205-291-30", "marketing_start_date": "20190701"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-60)", "package_ndc": "71205-291-60", "marketing_start_date": "20190701"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-291-90)", "package_ndc": "71205-291-90", "marketing_start_date": "20190701"}], "brand_name": "Bupropion Hydrochloride XL", "product_id": "71205-291_ee865180-23ee-4b72-a56e-30db9551dddc", "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": "71205-291", "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": "150 mg/1"}], "application_number": "ANDA207224", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}