Package 50090-4715-0

{"route": ["ORAL"], "spl_id": "71227eaa-30c6-43df-b625-f2afeb3a4cbf", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["ab58f3ef-1fd3-4c68-861f-20d8fdd1b433"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-4715-0)", "package_ndc": "50090-4715-0", "marketing_start_date": "20191112"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4715-1)", "package_ndc": "50090-4715-1", "marketing_start_date": "20191112"}], "brand_name": "venlafaxine", "product_id": "50090-4715_71227eaa-30c6-43df-b625-f2afeb3a4cbf", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "50090-4715", "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": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}