Package 69367-417-09

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 69367-417-09
Digits Only 6936741709
Product NDC 69367-417
Product ID 69367-417_f5372620-d970-4c76-b148-35264d890c1a
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)

Marketing

Marketing Status
Marketed Since 2025-11-18
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Venlafaxine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f5372620-d970-4c76-b148-35264d890c1a", "openfda": {"upc": ["0369367417099", "0369367418096"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748"], "spl_set_id": ["349308ef-2caf-4fec-b428-56ae06c6771d"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)", "package_ndc": "69367-417-09", "marketing_start_date": "20251118"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30)", "package_ndc": "69367-417-30", "marketing_start_date": "20251118"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "69367-417_f5372620-d970-4c76-b148-35264d890c1a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "69367-417", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205468", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}