Package 71335-1870-6

{"route": ["ORAL"], "spl_id": "d3e2b334-93f3-4a2b-bc31-8c03c2534ecd", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993536"], "spl_set_id": ["634bc654-be95-4fea-b308-eed53269a112"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-1)", "package_ndc": "71335-1870-1", "marketing_start_date": "20210524"}, {"sample": false, "description": "180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-2)", "package_ndc": "71335-1870-2", "marketing_start_date": "20240718"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-3)", "package_ndc": "71335-1870-3", "marketing_start_date": "20240718"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-4)", "package_ndc": "71335-1870-4", "marketing_start_date": "20240718"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-5)", "package_ndc": "71335-1870-5", "marketing_start_date": "20240718"}, {"sample": false, "description": "28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1870-6)", "package_ndc": "71335-1870-6", "marketing_start_date": "20240718"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "71335-1870_d3e2b334-93f3-4a2b-bc31-8c03c2534ecd", "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": "71335-1870", "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": "200 mg/1"}], "application_number": "ANDA211347", "marketing_category": "ANDA", "marketing_start_date": "20201102", "listing_expiration_date": "20261231"}