Package 60505-1317-3

Brand: paroxetine hydrochloride

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-1317-3
Digits Only 6050513173
Product NDC 60505-1317
Product ID 60505-1317_f641c7b3-f7d2-9446-e589-074ac368853a
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1317-3)

Marketing

Marketing Status
Marketed Since 2019-08-09
Brand paroxetine hydrochloride
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

PAROXETINE HYDROCHLORIDE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f641c7b3-f7d2-9446-e589-074ac368853a", "openfda": {"upc": ["0360505367436", "0360505367535", "0360505367337"], "unii": ["X2ELS050D8"], "rxcui": ["1738803", "1738805", "1738807"], "spl_set_id": ["087ff0d3-1761-47ea-a8c1-7c4cb679af97"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (60505-1317-3)", "package_ndc": "60505-1317-3", "marketing_start_date": "20190809"}], "brand_name": "PAROXETINE HYDROCHLORIDE", "product_id": "60505-1317_f641c7b3-f7d2-9446-e589-074ac368853a", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60505-1317", "generic_name": "paroxetine hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE HYDROCHLORIDE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "25 mg/1"}], "application_number": "NDA020936", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20190809", "listing_expiration_date": "20261231"}