Package 55700-621-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 55700-621-30
Digits Only 5570062130
Product NDC 55700-621
Description

30 TABLET, FILM COATED in 1 BOTTLE (55700-621-30)

Marketing

Marketing Status
Discontinued 2026-08-31
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": "bfce1454-2e1e-49fd-b252-3530480d140f", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["9460be93-cd53-4429-a4d9-2f04e3835168"], "manufacturer_name": ["Lake Erie Medical DBA Quality Care Products LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (55700-621-30)", "package_ndc": "55700-621-30", "marketing_end_date": "20260831", "marketing_start_date": "20180518"}], "brand_name": "Eszopiclone", "product_id": "55700-621_bfce1454-2e1e-49fd-b252-3530480d140f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "55700-621", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Lake Erie Medical DBA Quality Care Products LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA202929", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20180518"}