Package 68788-8752-6

{"route": ["ORAL"], "spl_id": "b16b2e74-763b-4b6b-8291-258d94bb9d9f", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["e2d5a2d5-5e55-426c-bc8d-d29729eba775"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8752-3)", "package_ndc": "68788-8752-3", "marketing_start_date": "20241014"}, {"sample": false, "description": "60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8752-6)", "package_ndc": "68788-8752-6", "marketing_start_date": "20241014"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68788-8752-9)", "package_ndc": "68788-8752-9", "marketing_start_date": "20241014"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "68788-8752_b16b2e74-763b-4b6b-8291-258d94bb9d9f", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68788-8752", "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": "ANDA200834", "marketing_category": "ANDA", "marketing_start_date": "20241014", "listing_expiration_date": "20271231"}