Package 68788-8072-9

{"route": ["ORAL"], "spl_id": "219c816d-9278-43e0-9a27-9f39cabee426", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["b18d726e-cdb2-4c80-a49d-330cddee17e9"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8072-3)", "package_ndc": "68788-8072-3", "marketing_start_date": "20210827"}, {"sample": false, "description": "500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8072-6)", "package_ndc": "68788-8072-6", "marketing_start_date": "20210827"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8072-9)", "package_ndc": "68788-8072-9", "marketing_start_date": "20210827"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8072_219c816d-9278-43e0-9a27-9f39cabee426", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8072", "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": "150 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20210827", "listing_expiration_date": "20261231"}