Package 80425-0477-1

{"route": ["ORAL"], "spl_id": "2d034ebe-1e07-6fe0-e063-6394a90a368b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808751"], "spl_set_id": ["2cf6e6ad-7d00-0db1-e063-6394a90ab1ec"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)", "package_ndc": "80425-0477-1", "marketing_start_date": "20250130"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)", "package_ndc": "80425-0477-2", "marketing_start_date": "20250130"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)", "package_ndc": "80425-0477-3", "marketing_start_date": "20250130"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "80425-0477_2d034ebe-1e07-6fe0-e063-6394a90a368b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0477", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "NDA022104", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250130", "listing_expiration_date": "20261231"}