Package 50090-5890-0

{"route": ["ORAL"], "spl_id": "708bf3c0-c834-43cc-9fab-d22a0615ffc9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581"], "spl_set_id": ["df7e0982-3eb0-4bdf-8f7f-4f4a48476ed7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-5890-0)", "package_ndc": "50090-5890-0", "marketing_start_date": "20220110"}, {"sample": false, "description": "90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-5890-1)", "package_ndc": "50090-5890-1", "marketing_start_date": "20220110"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "50090-5890_708bf3c0-c834-43cc-9fab-d22a0615ffc9", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-5890", "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": "150 mg/1"}], "application_number": "ANDA212277", "marketing_category": "ANDA", "marketing_start_date": "20190708", "listing_expiration_date": "20261231"}