Package 70710-1698-5

{"route": ["ORAL"], "spl_id": "9d291423-f1d9-4605-af7c-f18537aa8914", "openfda": {"upc": ["0370710170097", "0370710169992"], "unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313583", "313585"], "spl_set_id": ["9fda0f8d-b24e-4581-9dca-7aaaf86e2413"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-0)", "package_ndc": "70710-1698-0", "marketing_start_date": "20230518"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-3)", "package_ndc": "70710-1698-3", "marketing_start_date": "20230518"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70710-1698-4)  / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70710-1698-2)", "package_ndc": "70710-1698-4", "marketing_start_date": "20230518"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-5)", "package_ndc": "70710-1698-5", "marketing_start_date": "20230518"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70710-1698-9)", "package_ndc": "70710-1698-9", "marketing_start_date": "20230518"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70710-1698_9d291423-f1d9-4605-af7c-f18537aa8914", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70710-1698", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090174", "marketing_category": "ANDA", "marketing_start_date": "20230518", "listing_expiration_date": "20271231"}