Package 55289-053-90

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 55289-053-90
Digits Only 5528905390
Product NDC 55289-053
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-053-90)

Marketing

Marketing Status
Marketed Since 2011-04-01
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": "34663b6d-d8b7-08ea-e063-6294a90a6358", "openfda": {"upc": ["0355289053903"], "unii": ["X2ELS050D8"], "rxcui": ["1738511"], "spl_set_id": ["619e10bb-6e5d-4ec3-a85a-6270965f5389"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-053-45)", "package_ndc": "55289-053-45", "marketing_start_date": "20110401"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-053-90)", "package_ndc": "55289-053-90", "marketing_start_date": "20110401"}], "brand_name": "Paroxetine", "product_id": "55289-053_34663b6d-d8b7-08ea-e063-6294a90a6358", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "55289-053", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "40 mg/1"}], "application_number": "ANDA078902", "marketing_category": "ANDA", "marketing_start_date": "20080324", "listing_expiration_date": "20261231"}