Package 71335-1986-6

{"route": ["ORAL"], "spl_id": "81a9f421-c489-4306-a693-94e61aa30b39", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993503"], "spl_set_id": ["500fc18d-93b4-47d5-a3f7-3f68822d83e8"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-1)", "package_ndc": "71335-1986-1", "marketing_start_date": "20211104"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-2)", "package_ndc": "71335-1986-2", "marketing_start_date": "20240718"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-3)", "package_ndc": "71335-1986-3", "marketing_start_date": "20240718"}, {"sample": false, "description": "45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-4)", "package_ndc": "71335-1986-4", "marketing_start_date": "20240718"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-5)", "package_ndc": "71335-1986-5", "marketing_start_date": "20240718"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1986-6)", "package_ndc": "71335-1986-6", "marketing_start_date": "20221229"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "71335-1986_81a9f421-c489-4306-a693-94e61aa30b39", "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": "71335-1986", "generic_name": "bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA211347", "marketing_category": "ANDA", "marketing_start_date": "20201102", "listing_expiration_date": "20261231"}