Package 70518-4151-0

Brand: venlafaxine hydrochloride

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4151-0
Digits Only 7051841510
Product NDC 70518-4151
Product ID 70518-4151_3fb62823-b2ba-299d-e063-6294a90ac261
Description

30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4151-0)

Marketing

Marketing Status
Marketed Since 2024-07-29
Brand venlafaxine hydrochloride
Generic venlafaxine hydrochloride
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": "3fb62823-b2ba-299d-e063-6294a90ac261", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313585"], "spl_set_id": ["33b39416-7981-46fb-ba31-e933a6afcf8b"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70518-4151-0)", "package_ndc": "70518-4151-0", "marketing_start_date": "20240729"}], "brand_name": "Venlafaxine Hydrochloride", "product_id": "70518-4151_3fb62823-b2ba-299d-e063-6294a90ac261", "dosage_form": "CAPSULE, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-4151", "generic_name": "VENLAFAXINE HYDROCHLORIDE", "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": "ANDA214654", "marketing_category": "ANDA", "marketing_start_date": "20240729", "listing_expiration_date": "20261231"}