Package 80425-0471-1

{"route": ["ORAL"], "spl_id": "2c2ba237-e6f3-fe8b-e063-6294a90ad400", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["2c2bb0e6-5a73-ff57-e063-6294a90a88d3"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0471-1)", "package_ndc": "80425-0471-1", "marketing_start_date": "20250120"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0471-2)", "package_ndc": "80425-0471-2", "marketing_start_date": "20250120"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0471-3)", "package_ndc": "80425-0471-3", "marketing_start_date": "20250120"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "80425-0471_2c2ba237-e6f3-fe8b-e063-6294a90ad400", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0471", "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": "75 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20250120", "listing_expiration_date": "20261231"}