Package 68001-497-04

Brand: venlafaxine hydrochloride

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 68001-497-04
Digits Only 6800149704
Product NDC 68001-497
Product ID 68001-497_2b5c3dc6-9055-abe9-e063-6294a90af76e
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-497-04)

Marketing

Marketing Status
Marketed Since 2021-04-30
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": "2b5c3dc6-9055-abe9-e063-6294a90af76e", "openfda": {"upc": ["0368001499040", "0368001498043", "0368001496049", "0368001497046"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["5efe1336-c796-4560-8110-a64c80eefb0c"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68001-497-04)", "package_ndc": "68001-497-04", "marketing_start_date": "20210430"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "68001-497_2b5c3dc6-9055-abe9-e063-6294a90af76e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "68001-497", "generic_name": "venlafaxine", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA214419", "marketing_category": "ANDA", "marketing_start_date": "20210430", "listing_expiration_date": "20261231"}