Package 80425-0339-1

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 80425-0339-1
Digits Only 8042503391
Product NDC 80425-0339
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0339-1)

Marketing

Marketing Status
Marketed Since 2023-05-19
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a9bf7d3-46dd-0dfa-e063-6394a90a76a4", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738495"], "spl_set_id": ["fc11a056-7db5-1966-e053-6394a90aa59c"], "manufacturer_name": ["Advanced Rx Pharmacy of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0339-1)", "package_ndc": "80425-0339-1", "marketing_start_date": "20230519"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0339-2)", "package_ndc": "80425-0339-2", "marketing_start_date": "20230519"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0339-3)", "package_ndc": "80425-0339-3", "marketing_start_date": "20230519"}], "brand_name": "Paroxetine", "product_id": "80425-0339_2a9bf7d3-46dd-0dfa-e063-6394a90a76a4", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "80425-0339", "generic_name": "Paroxetine", "labeler_name": "Advanced Rx Pharmacy of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "20 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20230519", "listing_expiration_date": "20261231"}