eszopiclone
Generic: eszopiclone
Labeler: preferred pharmaceuticals inc.Drug Facts
Product Profile
Brand Name
eszopiclone
Generic Name
eszopiclone
Labeler
preferred pharmaceuticals inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
eszopiclone 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68788-8826
Product ID
68788-8826_be25bb4e-d84f-4396-a78f-a668a207cf2d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA202929
DEA Schedule
civ
Listing Expiration
2026-12-31
Marketing Start
2025-02-10
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
687888826
Hyphenated Format
68788-8826
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
eszopiclone (source: ndc)
Generic Name
eszopiclone (source: ndc)
Application Number
ANDA202929 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (68788-8826-3)
- 60 TABLET, FILM COATED in 1 BOTTLE (68788-8826-6)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "be25bb4e-d84f-4396-a78f-a668a207cf2d", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["be25bb4e-d84f-4396-a78f-a668a207cf2d"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-8826-3)", "package_ndc": "68788-8826-3", "marketing_start_date": "20250210"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-8826-6)", "package_ndc": "68788-8826-6", "marketing_start_date": "20250210"}], "brand_name": "Eszopiclone", "product_id": "68788-8826_be25bb4e-d84f-4396-a78f-a668a207cf2d", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-8826", "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": "ANDA202929", "marketing_category": "ANDA", "marketing_start_date": "20250210", "listing_expiration_date": "20261231"}