Package 50268-642-15

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 50268-642-15
Digits Only 5026864215
Product NDC 50268-642
Description

50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-642-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-642-11)

Marketing

Marketing Status
Marketed Since 2016-03-11
Brand paroxetine
Generic paroxetine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47442798-ab7c-7d4c-e063-6394a90a1082", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["d9a5e0aa-e638-5d6e-75c2-20cb78fc4f43"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-642-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-642-11)", "package_ndc": "50268-642-15", "marketing_start_date": "20160311"}], "brand_name": "Paroxetine", "product_id": "50268-642_47442798-ab7c-7d4c-e063-6394a90a1082", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "50268-642", "generic_name": "Paroxetine", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE HEMIHYDRATE", "strength": "30 mg/1"}], "application_number": "ANDA078406", "marketing_category": "ANDA", "marketing_start_date": "20160311", "listing_expiration_date": "20261231"}