Package 0591-3660-30

Brand: desvenlafaxine

Generic: desvenlafaxine
NDC Package

Package Facts

Identity

Package NDC 0591-3660-30
Digits Only 0591366030
Product NDC 0591-3660
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-3660-30)

Marketing

Marketing Status
Marketed Since 2017-03-01
Brand desvenlafaxine
Generic desvenlafaxine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9ae096b1-2fff-4410-b1c5-799171a05d54", "openfda": {"unii": ["ZB22ENF0XR"], "rxcui": ["1607617", "1874553", "1874559"], "spl_set_id": ["617476f9-62d7-40ef-a1b1-c349d4ad706f"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-3660-30)", "package_ndc": "0591-3660-30", "marketing_start_date": "20170301"}], "brand_name": "Desvenlafaxine", "product_id": "0591-3660_9ae096b1-2fff-4410-b1c5-799171a05d54", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Cytochrome P450 2D6 Inhibitors [MoA]", "Norepinephrine Uptake Inhibitors [MoA]", "Serotonin Uptake Inhibitors [MoA]", "Serotonin and Norepinephrine Reuptake Inhibitor [EPC]"], "product_ndc": "0591-3660", "generic_name": "Desvenlafaxine", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Desvenlafaxine", "active_ingredients": [{"name": "DESVENLAFAXINE SUCCINATE", "strength": "100 mg/1"}], "application_number": "ANDA204065", "marketing_category": "ANDA", "marketing_start_date": "20170301", "listing_expiration_date": "20261231"}