Package 51407-454-90
Brand: venlafaxine
Generic: venlafaxinePackage Facts
Identity
Package NDC
51407-454-90
Digits Only
5140745490
Product NDC
51407-454
Description
90 TABLET in 1 BOTTLE (51407-454-90)
Marketing
Marketing Status
Brand
venlafaxine
Generic
venlafaxine
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2426a1ee-c88e-1acc-e063-6394a90a2abb", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["c2a3283f-ba30-f506-e053-2995a90a9378"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (51407-454-90)", "package_ndc": "51407-454-90", "marketing_start_date": "20210402"}], "brand_name": "Venlafaxine", "product_id": "51407-454_2426a1ee-c88e-1acc-e063-6394a90a2abb", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51407-454", "generic_name": "Venlafaxine", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA078627", "marketing_category": "ANDA", "marketing_start_date": "20080613", "listing_expiration_date": "20261231"}