Package 65862-404-01

Brand: venlafaxine

Generic: venlafaxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65862-404-01
Digits Only 6586240401
Product NDC 65862-404
Description

100 TABLET in 1 BOTTLE (65862-404-01)

Marketing

Marketing Status
Marketed Since 2010-04-07
Brand venlafaxine
Generic venlafaxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "426d12db-50e2-4915-999f-84645fb387d9", "openfda": {"unii": ["7D7RX5A8MO"], "rxcui": ["313580", "313582", "313584", "313586", "314277"], "spl_set_id": ["b23637e5-d37f-41b5-ba76-fc053e903bc2"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-404-01)", "package_ndc": "65862-404-01", "marketing_start_date": "20100407"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-404-10)  / 10 TABLET in 1 BLISTER PACK", "package_ndc": "65862-404-10", "marketing_start_date": "20100407"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (65862-404-30)", "package_ndc": "65862-404-30", "marketing_start_date": "20100407"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (65862-404-60)", "package_ndc": "65862-404-60", "marketing_start_date": "20100407"}, {"sample": false, "description": "7000 TABLET in 1 BOTTLE (65862-404-71)", "package_ndc": "65862-404-71", "marketing_start_date": "20100407"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (65862-404-90)", "package_ndc": "65862-404-90", "marketing_start_date": "20100407"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-404-99)", "package_ndc": "65862-404-99", "marketing_start_date": "20100407"}], "brand_name": "Venlafaxine", "product_id": "65862-404_426d12db-50e2-4915-999f-84645fb387d9", "dosage_form": "TABLET", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "65862-404", "generic_name": "Venlafaxine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Venlafaxine", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA090555", "marketing_category": "ANDA", "marketing_start_date": "20100407", "listing_expiration_date": "20261231"}