Package 70518-4398-0

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 70518-4398-0
Digits Only 7051843980
Product NDC 70518-4398
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4398-0)

Marketing

Marketing Status
Marketed Since 2025-07-24
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3aaedc44-7250-b21e-e063-6394a90a2a93", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485442"], "spl_set_id": ["9dfe774a-2c7a-4e10-bedd-cde64ad28676"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4398-0)", "package_ndc": "70518-4398-0", "marketing_start_date": "20250724"}], "brand_name": "Eszopiclone", "product_id": "70518-4398_3aaedc44-7250-b21e-e063-6394a90a2a93", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4398", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "2 mg/1"}], "application_number": "ANDA202929", "marketing_category": "ANDA", "marketing_start_date": "20250724", "listing_expiration_date": "20261231"}