Package 71610-204-60

Brand: paroxetine

Generic: paroxetine hydrochloride hemihydrate
NDC Package

Package Facts

Identity

Package NDC 71610-204-60
Digits Only 7161020460
Product NDC 71610-204
Product ID 71610-204_127e7f93-615c-45d1-91a6-98091c1e2d81
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-204-60)

Marketing

Marketing Status
Marketed Since 2018-12-13
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": "127e7f93-615c-45d1-91a6-98091c1e2d81", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483"], "spl_set_id": ["2eebd2b6-7c64-45ca-8eb5-5201137f610a"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-204-60)", "package_ndc": "71610-204-60", "marketing_start_date": "20181213"}], "brand_name": "Paroxetine", "product_id": "71610-204_127e7f93-615c-45d1-91a6-98091c1e2d81", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "71610-204", "generic_name": "paroxetine hydrochloride hemihydrate", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "10 mg/1"}], "application_number": "ANDA078902", "marketing_category": "ANDA", "marketing_start_date": "20080324", "listing_expiration_date": "20261231"}