Package 68788-8694-6

{"route": ["ORAL"], "spl_id": "4b1326b9-f687-4444-a78a-e5617aced0ca", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["b055df74-51f9-401f-8cca-24269a0163df"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8694-3)", "package_ndc": "68788-8694-3", "marketing_start_date": "20240610"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8694-6)", "package_ndc": "68788-8694-6", "marketing_start_date": "20240610"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8694-9)", "package_ndc": "68788-8694-9", "marketing_start_date": "20240610"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8694_4b1326b9-f687-4444-a78a-e5617aced0ca", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8694", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20240610", "listing_expiration_date": "20261231"}