Package 70518-4065-0

Brand: venlafaxine hydrochloride

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 70518-4065-0
Digits Only 7051840650
Product NDC 70518-4065
Product ID 70518-4065_3fa2c2e6-f238-6e07-e063-6394a90a86d0
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4065-0)

Marketing

Marketing Status
Marketed Since 2024-05-04
Brand venlafaxine hydrochloride
Generic venlafaxine
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": "3fa2c2e6-f238-6e07-e063-6394a90a86d0", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["808753"], "spl_set_id": ["9df3a51c-1b89-4d2a-8f41-3755910e9bfb"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4065-0)", "package_ndc": "70518-4065-0", "marketing_start_date": "20240504"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-4065_3fa2c2e6-f238-6e07-e063-6394a90a86d0", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4065", "generic_name": "Venlafaxine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine Hydrochloride", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA216044", "marketing_category": "ANDA", "marketing_start_date": "20240504", "listing_expiration_date": "20261231"}