Package 69452-348-20

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 69452-348-20
Digits Only 6945234820
Product NDC 69452-348
Description

100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-348-20)

Marketing

Marketing Status
Marketed Since 2022-06-01
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": "903d952f-704a-4227-a829-5bddbd5793cb", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["ec6ac172-509e-403a-aa0d-4c60010a0035"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-348-20)", "package_ndc": "69452-348-20", "marketing_start_date": "20220601"}], "brand_name": "ESZOPICLONE", "product_id": "69452-348_903d952f-704a-4227-a829-5bddbd5793cb", "dosage_form": "TABLET, FILM COATED", "product_ndc": "69452-348", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "2 mg/1"}], "application_number": "ANDA091113", "marketing_category": "ANDA", "marketing_start_date": "20220601", "listing_expiration_date": "20261231"}