Package 70518-1310-0

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 70518-1310-0
Digits Only 7051813100
Product NDC 70518-1310
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1310-0)

Marketing

Marketing Status
Marketed Since 2018-07-18
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": "48d52a4e-6e91-e9e5-e063-6394a90a2a94", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485442"], "spl_set_id": ["7df922bc-5750-4259-906f-64f960c38d5f"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1310-0)", "package_ndc": "70518-1310-0", "marketing_start_date": "20180718"}], "brand_name": "ESZOPICLONE", "product_id": "70518-1310_48d52a4e-6e91-e9e5-e063-6394a90a2a94", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-1310", "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": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20180718", "listing_expiration_date": "20271231"}