Package 70518-4566-0

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 70518-4566-0
Digits Only 7051845660
Product NDC 70518-4566
Product ID 70518-4566_4a139303-d765-22b1-e063-6294a90aa507
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4566-0)

Marketing

Marketing Status
Marketed Since 2026-02-04
Brand venlafaxine
Generic venlafaxine
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4a139303-d765-22b1-e063-6294a90aa507", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808753"], "spl_set_id": ["570beece-6f30-4850-a3bc-636e7cf8d423"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4566-0)", "package_ndc": "70518-4566-0", "marketing_start_date": "20260204"}], "brand_name": "Venlafaxine", "product_id": "70518-4566_4a139303-d765-22b1-e063-6294a90aa507", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4566", "generic_name": "Venlafaxine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA215622", "marketing_category": "ANDA", "marketing_start_date": "20260204", "listing_expiration_date": "20271231"}