Package 50090-4853-0

{"route": ["ORAL"], "spl_id": "4858b2b3-fa81-4906-b002-5bb1d3bb100b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["5bd03cf1-e8fc-44f3-9c41-06515b897f3b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4853-0)", "package_ndc": "50090-4853-0", "marketing_start_date": "20200120"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4853-1)", "package_ndc": "50090-4853-1", "marketing_start_date": "20200120"}], "brand_name": "venlafaxine", "product_id": "50090-4853_4858b2b3-fa81-4906-b002-5bb1d3bb100b", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-4853", "generic_name": "venlafaxine hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}