Package 63629-9498-1

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 63629-9498-1
Digits Only 6362994981
Product NDC 63629-9498
Product ID 63629-9498_8053ba32-fceb-458d-898a-00ecf06b685d
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9498-1)

Marketing

Marketing Status
Discontinued 2026-07-31
Brand paroxetine
Generic paroxetine hydrochloride hemihydrate
Sample Package No

Linked Drug Pages (1)

PAROXETINE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8053ba32-fceb-458d-898a-00ecf06b685d", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738803"], "spl_set_id": ["27729943-8046-4342-af60-bc1da229abac"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9498-1)", "package_ndc": "63629-9498-1", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}], "brand_name": "PAROXETINE", "product_id": "63629-9498_8053ba32-fceb-458d-898a-00ecf06b685d", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-9498", "generic_name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PAROXETINE", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "12.5 mg/1"}], "application_number": "ANDA209293", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}