Package 68788-8068-6

{"route": ["ORAL"], "spl_id": "c59a3cd5-55ac-4cb2-9e63-325f42e0602e", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["653f3f95-98d0-4ce0-bf10-ac7938be690e"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8068-3)", "package_ndc": "68788-8068-3", "marketing_start_date": "20210823"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8068-6)", "package_ndc": "68788-8068-6", "marketing_start_date": "20210823"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8068-9)", "package_ndc": "68788-8068-9", "marketing_start_date": "20210823"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8068_c59a3cd5-55ac-4cb2-9e63-325f42e0602e", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8068", "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": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20210823", "listing_expiration_date": "20261231"}