Package 43063-795-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 43063-795-30
Digits Only 4306379530
Product NDC 43063-795
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-795-30)

Marketing

Marketing Status
Marketed Since 2017-10-09
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415b59ae-84e5-550f-e063-6294a90af226", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["4832cfbf-a540-46af-bb7d-3ba8e6bc783e"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-795-30)", "package_ndc": "43063-795-30", "marketing_start_date": "20171009"}], "brand_name": "Eszopiclone", "product_id": "43063-795_415b59ae-84e5-550f-e063-6294a90af226", "dosage_form": "TABLET, FILM COATED", "product_ndc": "43063-795", "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": "ANDA091124", "marketing_category": "ANDA", "marketing_start_date": "20140415", "listing_expiration_date": "20261231"}