Package 70518-3576-0
Brand: eszopiclone
Generic: eszopiclonePackage Facts
Identity
Package NDC
70518-3576-0
Digits Only
7051835760
Product NDC
70518-3576
Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3576-0)
Marketing
Marketing Status
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": "3ff0203e-da0b-cc72-e063-6294a90a0dc2", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["61fd4655-060f-4393-a610-019d8b127058"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3576-0)", "package_ndc": "70518-3576-0", "marketing_start_date": "20221110"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3576-1)", "package_ndc": "70518-3576-1", "marketing_start_date": "20250617"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3576-2)", "package_ndc": "70518-3576-2", "marketing_start_date": "20250929"}], "brand_name": "Eszopiclone", "product_id": "70518-3576_3ff0203e-da0b-cc72-e063-6294a90a0dc2", "dosage_form": "TABLET, FILM COATED", "product_ndc": "70518-3576", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA202929", "marketing_category": "ANDA", "marketing_start_date": "20221110", "listing_expiration_date": "20261231"}