Package 65841-099-01

Brand: paroxetine

Generic: paroxetine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 65841-099-01
Digits Only 6584109901
Product NDC 65841-099
Description

100 TABLET, FILM COATED in 1 BOTTLE (65841-099-01)

Marketing

Marketing Status
Marketed Since 2007-04-13
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": "ef5c1ef5-2884-4395-a65a-92591c986150", "openfda": {"unii": ["3I3T11UD2S"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["6d5fcdb2-4d84-4b20-87e3-58a43e567500"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-099-01)", "package_ndc": "65841-099-01", "marketing_start_date": "20070413"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65841-099-05)", "package_ndc": "65841-099-05", "marketing_start_date": "20070413"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65841-099-06)", "package_ndc": "65841-099-06", "marketing_start_date": "20070413"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65841-099-10)", "package_ndc": "65841-099-10", "marketing_start_date": "20070413"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65841-099-16)", "package_ndc": "65841-099-16", "marketing_start_date": "20070413"}], "brand_name": "Paroxetine", "product_id": "65841-099_ef5c1ef5-2884-4395-a65a-92591c986150", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65841-099", "generic_name": "Paroxetine Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE ANHYDROUS", "strength": "30 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20070413", "listing_expiration_date": "20261231"}