Package 70518-1385-3

{"route": ["ORAL"], "spl_id": "48fb8b01-4fa8-be3f-e063-6394a90a0659", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["4a82cef5-693e-46e9-90c4-bff753cdce37"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1385-0)", "package_ndc": "70518-1385-0", "marketing_start_date": "20180824"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-1385-1)", "package_ndc": "70518-1385-1", "marketing_start_date": "20181004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (70518-1385-3)", "package_ndc": "70518-1385-3", "marketing_start_date": "20231107"}], "brand_name": "venlafaxine", "product_id": "70518-1385_48fb8b01-4fa8-be3f-e063-6394a90a0659", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1385", "generic_name": "venlafaxine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "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": "20180824", "listing_expiration_date": "20271231"}