Package 80425-0098-1

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 80425-0098-1
Digits Only 8042500981
Product NDC 80425-0098
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0098-1)

Marketing

Marketing Status
Marketed Since 2014-04-15
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a996b2b-b5d8-65e7-e063-6394a90adeed", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["b39dc64d-adc9-742e-e053-2a95a90ad18b"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0098-1)", "package_ndc": "80425-0098-1", "marketing_start_date": "20140415"}], "brand_name": "Eszopiclone", "product_id": "80425-0098_2a996b2b-b5d8-65e7-e063-6394a90adeed", "dosage_form": "TABLET, FILM COATED", "product_ndc": "80425-0098", "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": "1 mg/1"}], "application_number": "ANDA091124", "marketing_category": "ANDA", "marketing_start_date": "20140415", "listing_expiration_date": "20261231"}