Package 68788-8589-9

{"route": ["ORAL"], "spl_id": "9595974f-21f6-426e-8833-ae1a79a50b4a", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["c0d92aa1-638d-44dd-a7f1-26bdbb1176ef"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8589-1)", "package_ndc": "68788-8589-1", "marketing_start_date": "20240220"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8589-3)", "package_ndc": "68788-8589-3", "marketing_start_date": "20240220"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8589-6)", "package_ndc": "68788-8589-6", "marketing_start_date": "20240220"}, {"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8589-8)", "package_ndc": "68788-8589-8", "marketing_start_date": "20240220"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8589-9)", "package_ndc": "68788-8589-9", "marketing_start_date": "20240220"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68788-8589_9595974f-21f6-426e-8833-ae1a79a50b4a", "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": "68788-8589", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA211020", "marketing_category": "ANDA", "marketing_start_date": "20240220", "listing_expiration_date": "20261231"}