Package 50090-6834-0

{"route": ["ORAL"], "spl_id": "6a4b8ce0-260c-43ce-9dad-49df32bcb274", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313583"], "spl_set_id": ["5a990dbd-f280-4caf-b950-4703ee98b230"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6834-0)", "package_ndc": "50090-6834-0", "marketing_start_date": "20231121"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-6834-1)", "package_ndc": "50090-6834-1", "marketing_start_date": "20231121"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-6834_6a4b8ce0-260c-43ce-9dad-49df32bcb274", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-6834", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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": "20220907", "listing_expiration_date": "20271231"}