Package 80425-0066-1

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 80425-0066-1
Digits Only 8042500661
Product NDC 80425-0066
Product ID 80425-0066_2a98f01a-8d9f-0770-e063-6294a90a7bab
Description

30 TABLET, FILM COATED in 1 BOTTLE (80425-0066-1)

Marketing

Marketing Status
Marketed Since 2016-09-15
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": "2a98f01a-8d9f-0770-e063-6294a90a7bab", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["af869866-0a11-1a05-e053-2a95a90acdb8"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0066-1)", "package_ndc": "80425-0066-1", "marketing_start_date": "20160915"}], "brand_name": "Eszopiclone", "product_id": "80425-0066_2a98f01a-8d9f-0770-e063-6294a90a7bab", "dosage_form": "TABLET, FILM COATED", "product_ndc": "80425-0066", "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": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}