Package 63629-9499-1

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 63629-9499-1
Digits Only 6362994991
Product NDC 63629-9499
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9499-1)

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c7051c2-7bef-402b-808d-1095f5eb52bd", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738805"], "spl_set_id": ["51189cf4-4122-48d4-b47f-4f98a8dfb8e0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-9499-1)", "package_ndc": "63629-9499-1", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}], "brand_name": "PAROXETINE", "product_id": "63629-9499_0c7051c2-7bef-402b-808d-1095f5eb52bd", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "63629-9499", "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": "25 mg/1"}], "application_number": "ANDA209293", "marketing_category": "ANDA", "marketing_end_date": "20260731", "marketing_start_date": "20180914"}