eszopiclone

Generic: eszopiclone

Labeler: bionpharma inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eszopiclone
Generic Name eszopiclone
Labeler bionpharma inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eszopiclone 2 mg/1

Manufacturer
Bionpharma Inc.

Identifiers & Regulatory

Product NDC 69452-348
Product ID 69452-348_903d952f-704a-4227-a829-5bddbd5793cb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091113
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2022-06-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69452348
Hyphenated Format 69452-348

Supplemental Identifiers

RxCUI
485440 485442 485465
UNII
UZX80K71OE

Packaging Origin

Original Packager
true

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 ANDA091113 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69452-348-20)
source: ndc

Packages (1)

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

Ingredients (1)

eszopiclone (2 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": "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"}