Package 82804-124-30

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 82804-124-30
Digits Only 8280412430
Product NDC 82804-124
Product ID 82804-124_470ad045-6c82-4e44-8e88-0e2b01a41ff2
Description

30 TABLET in 1 BOTTLE (82804-124-30)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "470ad045-6c82-4e44-8e88-0e2b01a41ff2", "openfda": {"upc": ["0382804124305"], "unii": ["7D7RX5A8MO"], "rxcui": ["313582"], "spl_set_id": ["470ad045-6c82-4e44-8e88-0e2b01a41ff2"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-124-30)", "package_ndc": "82804-124-30", "marketing_start_date": "20240716"}], "brand_name": "venlafaxine", "product_id": "82804-124_470ad045-6c82-4e44-8e88-0e2b01a41ff2", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "82804-124", "generic_name": "venlafaxine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}