Package 60505-4517-3

Brand: paxil

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-4517-3
Digits Only 6050545173
Product NDC 60505-4517
Description

30 TABLET, FILM COATED in 1 BOTTLE (60505-4517-3)

Marketing

Marketing Status
Marketed Since 2019-03-11
Brand paxil
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "62b4ffe1-48e2-6dd5-d7ca-28e8efe36686", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["207349", "207350", "211699", "211700", "1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["ef3b5cbe-f9e1-c1ac-79da-cfe14e3a7e7e"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-4517-3)", "package_ndc": "60505-4517-3", "marketing_start_date": "20190311"}], "brand_name": "PAXIL", "product_id": "60505-4517_62b4ffe1-48e2-6dd5-d7ca-28e8efe36686", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60505-4517", "generic_name": "paroxetine hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAXIL", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA020031", "marketing_category": "NDA", "marketing_start_date": "20190311", "listing_expiration_date": "20261231"}