Package 70518-4361-1

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 70518-4361-1
Digits Only 7051843611
Product NDC 70518-4361
Product ID 70518-4361_3f2870c4-2c3c-d0f3-e063-6294a90aeac9
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4361-1)

Marketing

Marketing Status
Marketed Since 2025-09-19
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": "3f2870c4-2c3c-d0f3-e063-6294a90aeac9", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485442"], "spl_set_id": ["52ab8ee9-a04d-4e27-b0f4-eb050f144715"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4361-0)", "package_ndc": "70518-4361-0", "marketing_start_date": "20250617"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4361-1)", "package_ndc": "70518-4361-1", "marketing_start_date": "20250919"}], "brand_name": "Eszopiclone", "product_id": "70518-4361_3f2870c4-2c3c-d0f3-e063-6294a90aeac9", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-4361", "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": "ANDA205504", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}