Package 70518-1976-0

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-1976-0
Digits Only 7051819760
Product NDC 70518-1976
Product ID 70518-1976_498b6298-4087-3291-e063-6294a90ab68b
Description

30 TABLET in 1 BLISTER PACK (70518-1976-0)

Marketing

Marketing Status
Marketed Since 2019-03-25
Brand venlafaxine
Generic venlafaxine hydrochloride
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": "498b6298-4087-3291-e063-6294a90ab68b", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580"], "spl_set_id": ["806b3e38-3b2a-4aaa-973c-e2d921bb353e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1976-0)", "package_ndc": "70518-1976-0", "marketing_start_date": "20190325"}], "brand_name": "venlafaxine", "product_id": "70518-1976_498b6298-4087-3291-e063-6294a90ab68b", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "70518-1976", "generic_name": "venlafaxine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20190325", "listing_expiration_date": "20271231"}