Package 0615-8510-39

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0615-8510-39
Digits Only 0615851039
Product NDC 0615-8510
Product ID 0615-8510_f4c48a47-b134-4ed0-a838-0af90d59dc5d
Description

30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8510-39)

Marketing

Marketing Status
Marketed Since 2024-05-16
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": "f4c48a47-b134-4ed0-a838-0af90d59dc5d", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313581", "313585"], "spl_set_id": ["9c061460-3b80-41e1-a87a-1a25108ff740"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8510-39)", "package_ndc": "0615-8510-39", "marketing_start_date": "20240516"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "0615-8510_f4c48a47-b134-4ed0-a838-0af90d59dc5d", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0615-8510", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA217390", "marketing_category": "ANDA", "marketing_start_date": "20230925", "listing_expiration_date": "20261231"}