Package 57237-173-01

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 57237-173-01
Digits Only 5723717301
Product NDC 57237-173
Product ID 57237-173_4da7fe70-bb28-43f2-97b6-66d130e6c72f
Description

100 TABLET in 1 BOTTLE (57237-173-01)

Marketing

Marketing Status
Marketed Since 2010-04-07
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": "4da7fe70-bb28-43f2-97b6-66d130e6c72f", "openfda": {"upc": ["0357237176900", "0357237172902", "0357237174906", "0357237175903", "0357237173909"], "unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["20319949-ccf9-477a-a6e3-53502772deb9"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (57237-173-01)", "package_ndc": "57237-173-01", "marketing_start_date": "20100407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (57237-173-90)", "package_ndc": "57237-173-90", "marketing_start_date": "20100407"}], "brand_name": "venlafaxine", "product_id": "57237-173_4da7fe70-bb28-43f2-97b6-66d130e6c72f", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "57237-173", "generic_name": "venlafaxine hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20100407", "listing_expiration_date": "20261231"}