Package 71335-2469-1

{"route": ["ORAL"], "spl_id": "0c3952f8-d149-4812-bec9-ecf841fe1950", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["af5b1cc8-f078-4a7b-b64a-4cb2de1e5721"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-1)", "package_ndc": "71335-2469-1", "marketing_start_date": "20241112"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-2)", "package_ndc": "71335-2469-2", "marketing_start_date": "20241112"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-3)", "package_ndc": "71335-2469-3", "marketing_start_date": "20241112"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-4)", "package_ndc": "71335-2469-4", "marketing_start_date": "20241112"}, {"sample": false, "description": "14 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2469-5)", "package_ndc": "71335-2469-5", "marketing_start_date": "20241112"}], "brand_name": "Bupropion hydrochloride", "product_id": "71335-2469_0c3952f8-d149-4812-bec9-ecf841fe1950", "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": "71335-2469", "generic_name": "Bupropion hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA215568", "marketing_category": "ANDA", "marketing_start_date": "20221215", "listing_expiration_date": "20261231"}