Package 68788-8837-9

{"route": ["ORAL"], "spl_id": "15c77ad7-7edc-4c36-ba3f-3ef05dfb12dc", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["15c77ad7-7edc-4c36-ba3f-3ef05dfb12dc"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8837-3)", "package_ndc": "68788-8837-3", "marketing_start_date": "20250227"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8837-6)", "package_ndc": "68788-8837-6", "marketing_start_date": "20250227"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8837-9)", "package_ndc": "68788-8837-9", "marketing_start_date": "20250227"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8837_15c77ad7-7edc-4c36-ba3f-3ef05dfb12dc", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8837", "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": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}