Package 51655-717-52

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 51655-717-52
Digits Only 5165571752
Product NDC 51655-717
Product ID 51655-717_49510f70-d80c-1582-e063-6394a90a6da1
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-717-52)

Marketing

Marketing Status
Marketed Since 2021-05-26
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

venlafaxine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49510f70-d80c-1582-e063-6394a90a6da1", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580"], "spl_set_id": ["db5f1693-ca64-7a97-e053-2995a90acbff"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-717-52)", "package_ndc": "51655-717-52", "marketing_start_date": "20210526"}], "brand_name": "venlafaxine", "product_id": "51655-717_49510f70-d80c-1582-e063-6394a90a6da1", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51655-717", "generic_name": "venlafaxine", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20210526", "listing_expiration_date": "20271231"}