Package 60505-0083-1

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60505-0083-1
Digits Only 6050500831
Product NDC 60505-0083
Description

30 TABLET, FILM COATED in 1 BOTTLE (60505-0083-1)

Marketing

Marketing Status
Marketed Since 2003-09-08
Brand paroxetine
Generic paroxetine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "9cde2ef4-fd50-ed21-0628-cb6cd8a6153f", "openfda": {"upc": ["0360505010110", "0360505008414", "0360505009718", "0360505008315"], "unii": ["3I3T11UD2S"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["08320ea3-8f93-6f04-5d1c-f69af3eb5a81"], "manufacturer_name": ["Apotex Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-0083-1)", "package_ndc": "60505-0083-1", "marketing_start_date": "20030908"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60505-0083-2)", "package_ndc": "60505-0083-2", "marketing_start_date": "20030908"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-0083-4)", "package_ndc": "60505-0083-4", "marketing_start_date": "20030908"}], "brand_name": "PAROXETINE", "product_id": "60505-0083_9cde2ef4-fd50-ed21-0628-cb6cd8a6153f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "60505-0083", "generic_name": "paroxetine hydrochloride", "labeler_name": "Apotex Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "20 mg/1"}], "application_number": "ANDA075356", "marketing_category": "ANDA", "marketing_start_date": "20030908", "listing_expiration_date": "20261231"}