eszopiclone

Generic: eszopiclone

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eszopiclone
Generic Name eszopiclone
Labeler direct rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eszopiclone 1 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-099
Product ID 72189-099_2be80953-8e55-14bd-e063-6294a90a4fae
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091124
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2020-06-10

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189099
Hyphenated Format 72189-099

Supplemental Identifiers

RxCUI
485440
UNII
UZX80K71OE

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 ANDA091124 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)
  • 90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)
source: ndc

Packages (2)

72189-099-30 30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30) 72189-099-90 90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)

Ingredients (1)

eszopiclone (1 mg/1)

Linked Drug Pages (1)

ESZOPICLONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2be80953-8e55-14bd-e063-6294a90a4fae", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["a7bd3e3c-26e9-07e7-e053-2995a90a9ca5"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72189-099-30)", "package_ndc": "72189-099-30", "marketing_start_date": "20200610"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-099-90)", "package_ndc": "72189-099-90", "marketing_start_date": "20200610"}], "brand_name": "ESZOPICLONE", "product_id": "72189-099_2be80953-8e55-14bd-e063-6294a90a4fae", "dosage_form": "TABLET, FILM COATED", "product_ndc": "72189-099", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA091124", "marketing_category": "ANDA", "marketing_start_date": "20200610", "listing_expiration_date": "20261231"}