Package 70518-4500-0

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 70518-4500-0
Digits Only 7051845000
Product NDC 70518-4500
Product ID 70518-4500_4109ea54-b204-364e-e063-6394a90a0b9a
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)

Marketing

Marketing Status
Marketed Since 2025-10-12
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": "4109ea54-b204-364e-e063-6394a90a0b9a", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808744"], "spl_set_id": ["4b23e4bd-b6ab-42f2-b389-0be0b7e11b92"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4500-0)", "package_ndc": "70518-4500-0", "marketing_start_date": "20251012"}], "brand_name": "Venlafaxine", "product_id": "70518-4500_4109ea54-b204-364e-e063-6394a90a0b9a", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4500", "generic_name": "Venlafaxine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA214127", "marketing_category": "ANDA", "marketing_start_date": "20251012", "listing_expiration_date": "20261231"}