Package 72241-077-22

{"route": ["ORAL"], "spl_id": "14b38374-7287-47dd-8ef9-e88bd5b23a26", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808753"], "spl_set_id": ["14b38374-7287-47dd-8ef9-e88bd5b23a26"], "manufacturer_name": ["Modavar Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72241-077-04)", "package_ndc": "72241-077-04", "marketing_start_date": "20180816"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (72241-077-11)", "package_ndc": "72241-077-11", "marketing_start_date": "20180816"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72241-077-22)", "package_ndc": "72241-077-22", "marketing_start_date": "20180816"}], "brand_name": "Venlafaxine", "product_id": "72241-077_14b38374-7287-47dd-8ef9-e88bd5b23a26", "dosage_form": "TABLET, COATED", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72241-077", "generic_name": "Venlafaxine", "labeler_name": "Modavar Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA211323", "marketing_category": "ANDA", "marketing_start_date": "20180105", "listing_expiration_date": "20261231"}