Package 0378-5270-01

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 0378-5270-01
Digits Only 0378527001
Product NDC 0378-5270
Product ID 0378-5270_850bc29d-2353-4e1f-bfe4-0811eb79000f
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5270-01)

Marketing

Marketing Status
Marketed Since 2013-03-26
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": "850bc29d-2353-4e1f-bfe4-0811eb79000f", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["5469cc59-78f9-447a-9c33-12553bb4073d"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5270-01)", "package_ndc": "0378-5270-01", "marketing_start_date": "20130326"}], "brand_name": "Eszopiclone", "product_id": "0378-5270_850bc29d-2353-4e1f-bfe4-0811eb79000f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0378-5270", "dea_schedule": "CIV", "generic_name": "eszopiclone", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA091151", "marketing_category": "ANDA", "marketing_start_date": "20130326", "listing_expiration_date": "20261231"}