Package 68071-3643-9

Brand: venlafaxine

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68071-3643-9
Digits Only 6807136439
Product NDC 68071-3643
Product ID 68071-3643_1ce8f03a-6916-908c-e063-6394a90a270c
Description

90 TABLET in 1 BOTTLE (68071-3643-9)

Marketing

Marketing Status
Marketed Since 2024-07-10
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": "1ce8f03a-6916-908c-e063-6394a90a270c", "openfda": {"upc": ["0368071364392"], "unii": ["7D7RX5A8MO"], "rxcui": ["313586"], "spl_set_id": ["1ce9121b-aaa0-a5bb-e063-6394a90a2f3c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3643-9)", "package_ndc": "68071-3643-9", "marketing_start_date": "20240710"}], "brand_name": "venlafaxine", "product_id": "68071-3643_1ce8f03a-6916-908c-e063-6394a90a270c", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68071-3643", "generic_name": "venlafaxine", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA078932", "marketing_category": "ANDA", "marketing_start_date": "20151001", "listing_expiration_date": "20261231"}