Package 68084-046-01

Brand: paroxetine

Generic: paroxetine
NDC Package

Package Facts

Identity

Package NDC 68084-046-01
Digits Only 6808404601
Product NDC 68084-046
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-046-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-046-11)

Marketing

Marketing Status
Marketed Since 2005-03-15
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": "3f163cc0-999c-9fdd-e063-6394a90ac15e", "openfda": {"unii": ["X2ELS050D8"], "rxcui": ["1738483", "1738495", "1738503", "1738511"], "spl_set_id": ["b5a8f864-a53d-48d9-aca6-6b64017fb168"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-046-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-046-11)", "package_ndc": "68084-046-01", "marketing_start_date": "20050315"}], "brand_name": "Paroxetine", "product_id": "68084-046_3f163cc0-999c-9fdd-e063-6394a90ac15e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68084-046", "generic_name": "Paroxetine", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paroxetine", "active_ingredients": [{"name": "PAROXETINE HYDROCHLORIDE", "strength": "30 mg/1"}], "application_number": "ANDA077584", "marketing_category": "ANDA", "marketing_start_date": "20050315", "listing_expiration_date": "20261231"}