Package 72865-200-90

Brand: venlafaxine hydrochloride

Generic: venlafaxine
NDC Package

Package Facts

Identity

Package NDC 72865-200-90
Digits Only 7286520090
Product NDC 72865-200
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-200-90)

Marketing

Marketing Status
Marketed Since 2021-02-26
Brand venlafaxine hydrochloride
Generic venlafaxine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2cdc9267-9619-474a-abe4-a0b85ac3fb2d", "openfda": {"upc": ["0372865198902", "0372865199909", "0372865197301", "0372865198308", "0372865200308", "0372865200902", "0372865199305", "0372865197905"], "unii": ["7D7RX5A8MO"], "rxcui": ["808744", "808748", "808751", "808753"], "spl_set_id": ["68f40801-d35e-464e-ac94-21016b617ea2"], "manufacturer_name": ["XLCare Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-200-30)", "package_ndc": "72865-200-30", "marketing_start_date": "20210226"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72865-200-90)", "package_ndc": "72865-200-90", "marketing_start_date": "20210226"}], "brand_name": "VENLAFAXINE HYDROCHLORIDE", "product_id": "72865-200_2cdc9267-9619-474a-abe4-a0b85ac3fb2d", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "72865-200", "generic_name": "venlafaxine", "labeler_name": "XLCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VENLAFAXINE HYDROCHLORIDE", "active_ingredients": [{"name": "VENLAFAXINE HYDROCHLORIDE", "strength": "225 mg/1"}], "application_number": "ANDA214419", "marketing_category": "ANDA", "marketing_start_date": "20210226", "listing_expiration_date": "20261231"}