Package 50090-2408-0

{"route": ["ORAL"], "spl_id": "5839cd0a-2686-4b5c-9cf3-7992978d5146", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["d3475ce0-1368-4961-a9b9-44c5c33cdc58"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-2408-0)", "package_ndc": "50090-2408-0", "marketing_start_date": "20160519"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-2408-1)", "package_ndc": "50090-2408-1", "marketing_start_date": "20160519"}], "brand_name": "Venlafaxine", "product_id": "50090-2408_5839cd0a-2686-4b5c-9cf3-7992978d5146", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-2408", "generic_name": "Venlafaxine", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA077653", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}