Package 80425-0063-1

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 80425-0063-1
Digits Only 8042500631
Product NDC 80425-0063
Product ID 80425-0063_2a98ff70-0364-7169-e063-6394a90adc74
Description

60 TABLET, FILM COATED in 1 BOTTLE (80425-0063-1)

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": "2a98ff70-0364-7169-e063-6394a90adc74", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485442"], "spl_set_id": ["af86fca8-571e-0cac-e053-2a95a90ae402"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0063-1)", "package_ndc": "80425-0063-1", "marketing_start_date": "20160915"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0063-2)", "package_ndc": "80425-0063-2", "marketing_start_date": "20160915"}], "brand_name": "Eszopiclone", "product_id": "80425-0063_2a98ff70-0364-7169-e063-6394a90adc74", "dosage_form": "TABLET, FILM COATED", "product_ndc": "80425-0063", "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": "2 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}