Package 58151-125-93

{"route": ["ORAL"], "spl_id": "2319042f-5d24-42d3-9b0a-8893bed66813", "openfda": {"upc": ["0358151126934", "0358151125937", "0358151127931"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585", "729929", "729931", "729932"], "spl_set_id": ["c848a5d8-ba94-4c84-80e3-0bf35fb8e32e"], "manufacturer_name": ["Viatris Specialty LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-77)", "package_ndc": "58151-125-77", "marketing_start_date": "20240717"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (58151-125-93)", "package_ndc": "58151-125-93", "marketing_start_date": "20240717"}], "brand_name": "Effexor XR", "product_id": "58151-125_2319042f-5d24-42d3-9b0a-8893bed66813", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "58151-125", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Viatris Specialty LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Effexor", "brand_name_suffix": "XR", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "NDA020699", "marketing_category": "NDA", "marketing_start_date": "20240717", "listing_expiration_date": "20261231"}