Package 51655-323-52

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-323-52
Digits Only 5165532352
Product NDC 51655-323
Product ID 51655-323_48eafbab-f3bb-58cd-e063-6394a90a1544
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)

Marketing

Marketing Status
Marketed Since 2023-05-02
Brand venlafaxine
Generic venlafaxine hydrochloride
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": "48eafbab-f3bb-58cd-e063-6394a90a1544", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["fb076577-b9da-c78b-e053-6394a90a107b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)", "package_ndc": "51655-323-52", "marketing_start_date": "20230502"}], "brand_name": "venlafaxine", "product_id": "51655-323_48eafbab-f3bb-58cd-e063-6394a90a1544", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51655-323", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "37.5 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20230502", "listing_expiration_date": "20271231"}