Package 51655-332-52

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 51655-332-52
Digits Only 5165533252
Product NDC 51655-332
Product ID 51655-332_48eb112c-b597-7c26-e063-6394a90a4bf2
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-332-52)

Marketing

Marketing Status
Marketed Since 2021-06-10
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": "48eb112c-b597-7c26-e063-6394a90a4bf2", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313584"], "spl_set_id": ["dabfa0f2-0060-f0ee-e053-2a95a90aec9b"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-332-52)", "package_ndc": "51655-332-52", "marketing_start_date": "20210610"}], "brand_name": "venlafaxine", "product_id": "51655-332_48eb112c-b597-7c26-e063-6394a90a4bf2", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "51655-332", "generic_name": "venlafaxine", "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": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20210610", "listing_expiration_date": "20271231"}