Package 68788-8682-3

{"route": ["ORAL"], "spl_id": "96b77279-4664-43cc-ae1e-dd893b00c6d2", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["92b3f73d-d6ca-4d7d-9035-5700f527cb85"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-1)", "package_ndc": "68788-8682-1", "marketing_start_date": "20240601"}, {"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-3)", "package_ndc": "68788-8682-3", "marketing_start_date": "20240601"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-6)", "package_ndc": "68788-8682-6", "marketing_start_date": "20240601"}, {"sample": false, "description": "120 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-8)", "package_ndc": "68788-8682-8", "marketing_start_date": "20240601"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8682-9)", "package_ndc": "68788-8682-9", "marketing_start_date": "20240601"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8682_96b77279-4664-43cc-ae1e-dd893b00c6d2", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8682", "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": "37.5 mg/1"}], "application_number": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20240601", "listing_expiration_date": "20261231"}