Package 71610-409-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 71610-409-30
Digits Only 7161040930
Product NDC 71610-409
Description

30 TABLET, FILM COATED in 1 BOTTLE (71610-409-30)

Marketing

Marketing Status
Marketed Since 2020-03-26
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": "fa699b0f-cb02-4a27-b97a-80221ebeabed", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["9bbf260f-3090-46b5-b3ef-81174697f166"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-409-30)", "package_ndc": "71610-409-30", "marketing_start_date": "20200326"}], "brand_name": "Eszopiclone", "product_id": "71610-409_fa699b0f-cb02-4a27-b97a-80221ebeabed", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71610-409", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA091169", "marketing_category": "ANDA", "marketing_start_date": "20140414", "listing_expiration_date": "20261231"}