Package 80425-0472-1

{"route": ["ORAL"], "spl_id": "2a7d4463-bf69-ce46-e063-6294a90a4722", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["2a7d760c-fd9f-8026-e063-6294a90aaa43"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0472-1)", "package_ndc": "80425-0472-1", "marketing_start_date": "20241230"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0472-2)", "package_ndc": "80425-0472-2", "marketing_start_date": "20241230"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (80425-0472-3)", "package_ndc": "80425-0472-3", "marketing_start_date": "20241230"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "80425-0472_2a7d4463-bf69-ce46-e063-6294a90a4722", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "80425-0472", "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": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20241230", "listing_expiration_date": "20261231"}