Package 68788-8825-3

{"route": ["ORAL"], "spl_id": "edefc932-d25d-4ead-b348-b3b6d9232091", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808753"], "spl_set_id": ["edefc932-d25d-4ead-b348-b3b6d9232091"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-3)", "package_ndc": "68788-8825-3", "marketing_start_date": "20250210"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-6)", "package_ndc": "68788-8825-6", "marketing_start_date": "20250210"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8825-9)", "package_ndc": "68788-8825-9", "marketing_start_date": "20250210"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8825_edefc932-d25d-4ead-b348-b3b6d9232091", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8825", "generic_name": "Venlafaxine", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA216044", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}