Package 68788-8387-3

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 68788-8387-3
Digits Only 6878883873
Product NDC 68788-8387
Description

30 TABLET, FILM COATED in 1 BOTTLE (68788-8387-3)

Marketing

Marketing Status
Marketed Since 2023-03-01
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": "e98c3608-86e2-46b9-97fc-93663f53c86d", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["0102ea59-77b1-4e74-83ec-1d205563b55f"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8387-3)", "package_ndc": "68788-8387-3", "marketing_start_date": "20230301"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8387-6)", "package_ndc": "68788-8387-6", "marketing_start_date": "20230301"}], "brand_name": "Eszopiclone", "product_id": "68788-8387_e98c3608-86e2-46b9-97fc-93663f53c86d", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-8387", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA091166", "marketing_category": "ANDA", "marketing_start_date": "20230301", "listing_expiration_date": "20261231"}