Package 69117-0027-5

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 69117-0027-5
Digits Only 6911700275
Product NDC 69117-0027
Description

1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-5)

Marketing

Marketing Status
Marketed Since 2021-11-02
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": "472863af-ee04-24a6-e063-6394a90a9e20", "openfda": {"upc": ["0369117002612", "0369117002438", "0369117002735", "0369117002537", "0369117002445", "0369117002728", "0369117002636", "0369117002643", "0369117002520", "0369117002452", "0369117002414", "0369117002759", "0369117002421", "0369117002650", "0369117002551", "0369117002742", "0369117002513", "0369117002544", "0369117002711"], "unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["4abd94c5-5ad5-4a43-9c51-a93ea1c1f3bc"], "manufacturer_name": ["Yiling Pharmaceutical, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-1)", "package_ndc": "69117-0027-1", "marketing_start_date": "20211102"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-2)", "package_ndc": "69117-0027-2", "marketing_start_date": "20211102"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-3)", "package_ndc": "69117-0027-3", "marketing_start_date": "20211102"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-4)", "package_ndc": "69117-0027-4", "marketing_start_date": "20211102"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69117-0027-5)", "package_ndc": "69117-0027-5", "marketing_start_date": "20211102"}], "brand_name": "Paroxetine", "product_id": "69117-0027_472863af-ee04-24a6-e063-6394a90a9e20", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "69117-0027", "generic_name": "Paroxetine", "labeler_name": "Yiling Pharmaceutical, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "40 mg/1"}], "application_number": "ANDA211248", "marketing_category": "ANDA", "marketing_start_date": "20211102", "listing_expiration_date": "20261231"}