Package 68382-019-16

{"route": ["ORAL"], "spl_id": "ea404f6c-7e07-4779-a52c-8cffb92718ef", "openfda": {"upc": ["0368382019011", "0368382018014", "0368382021014", "0368382101013"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["72efad5f-0909-46a5-aa13-ac24fe015fe6"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-019-01)", "package_ndc": "68382-019-01", "marketing_start_date": "20080613"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-019-05)", "package_ndc": "68382-019-05", "marketing_start_date": "20080613"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68382-019-06)", "package_ndc": "68382-019-06", "marketing_start_date": "20080613"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-019-10)", "package_ndc": "68382-019-10", "marketing_start_date": "20080613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68382-019-14)", "package_ndc": "68382-019-14", "marketing_start_date": "20080613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-019-16)", "package_ndc": "68382-019-16", "marketing_start_date": "20080613"}], "brand_name": "Venlafaxine", "product_id": "68382-019_ea404f6c-7e07-4779-a52c-8cffb92718ef", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68382-019", "generic_name": "Venlafaxine", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}