Package 72189-099-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 72189-099-30
Digits Only 7218909930
Product NDC 72189-099
Product ID 72189-099_2be80953-8e55-14bd-e063-6294a90a4fae
Description

30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)

Marketing

Marketing Status
Marketed Since 2020-06-10
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": "2be80953-8e55-14bd-e063-6294a90a4fae", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["a7bd3e3c-26e9-07e7-e053-2995a90a9ca5"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)", "package_ndc": "72189-099-30", "marketing_start_date": "20200610"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)", "package_ndc": "72189-099-90", "marketing_start_date": "20200610"}], "brand_name": "ESZOPICLONE", "product_id": "72189-099_2be80953-8e55-14bd-e063-6294a90a4fae", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72189-099", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "DIRECT RX", "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": "20200610", "listing_expiration_date": "20261231"}