Package 0615-8359-39

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 0615-8359-39
Digits Only 0615835939
Product NDC 0615-8359
Product ID 0615-8359_d04ea3ee-ed50-48ca-8226-fb2d029053f3
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8359-39)

Marketing

Marketing Status
Marketed Since 2020-11-11
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Paroxetine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d04ea3ee-ed50-48ca-8226-fb2d029053f3", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["0a8a58c7-5008-4c65-ae0e-e4ee809b1807"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8359-39)", "package_ndc": "0615-8359-39", "marketing_start_date": "20201111"}], "brand_name": "Paroxetine", "product_id": "0615-8359_d04ea3ee-ed50-48ca-8226-fb2d029053f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8359", "generic_name": "Paroxetine", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078406", "marketing_category": "ANDA", "marketing_start_date": "20091203", "listing_expiration_date": "20261231"}