Package 65841-671-14

{"route": ["ORAL"], "spl_id": "d4325db5-166d-4719-bdbd-a89ef8c96833", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["51334651-7a7f-4653-bf9d-d5be04fd902d"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65841-671-01)", "package_ndc": "65841-671-01", "marketing_start_date": "20080613"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (65841-671-05)", "package_ndc": "65841-671-05", "marketing_start_date": "20080613"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65841-671-06)", "package_ndc": "65841-671-06", "marketing_start_date": "20080613"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65841-671-10)", "package_ndc": "65841-671-10", "marketing_start_date": "20080613"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65841-671-14)", "package_ndc": "65841-671-14", "marketing_start_date": "20080613"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65841-671-16)", "package_ndc": "65841-671-16", "marketing_start_date": "20080613"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "65841-671_d4325db5-166d-4719-bdbd-a89ef8c96833", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65841-671", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}