Package 80425-0065-1

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 80425-0065-1
Digits Only 8042500651
Product NDC 80425-0065
Product ID 80425-0065_2a98d9c1-b772-40b1-e063-6294a90a20e4
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0065-1)

Marketing

Marketing Status
Marketed Since 2014-04-25
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (1)

Eszopiclone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a98d9c1-b772-40b1-e063-6294a90a20e4", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["af863d89-25db-2893-e053-2a95a90a704c"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0065-1)", "package_ndc": "80425-0065-1", "marketing_start_date": "20140425"}], "brand_name": "Eszopiclone", "product_id": "80425-0065_2a98d9c1-b772-40b1-e063-6294a90a20e4", "dosage_form": "TABLET, FILM COATED", "product_ndc": "80425-0065", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA202929", "marketing_category": "ANDA", "marketing_start_date": "20140425", "listing_expiration_date": "20261231"}