Package 72789-067-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 72789-067-30
Digits Only 7278906730
Product NDC 72789-067
Product ID 72789-067_403149fb-ab38-8d11-e063-6294a90a14a9
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-067-30)

Marketing

Marketing Status
Marketed Since 2020-03-26
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": "403149fb-ab38-8d11-e063-6294a90a14a9", "openfda": {"upc": ["0372789067308"], "unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["bb972d36-4b2c-45ae-8504-3a16d352dd8b"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-067-30)", "package_ndc": "72789-067-30", "marketing_start_date": "20200326"}], "brand_name": "ESZOPICLONE", "product_id": "72789-067_403149fb-ab38-8d11-e063-6294a90a14a9", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72789-067", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}