eszopiclone

Generic: eszopiclone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eszopiclone
Generic Name eszopiclone
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eszopiclone 1 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0598
Product ID 71335-0598_1cede81a-b1b6-4a31-bba8-9f7d483d2292
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202929
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2015-01-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350598
Hyphenated Format 71335-0598

Supplemental Identifiers

RxCUI
485440 485442 485465
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 ANDA202929 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0598-1)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0598-2)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0598-3)
  • 10 TABLET, FILM COATED in 1 BOTTLE (71335-0598-4)
  • 120 TABLET, FILM COATED in 1 BOTTLE (71335-0598-5)
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0598-6)
source: ndc

Packages (6)

71335-0598-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0598-1) 71335-0598-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-0598-2) 71335-0598-3 90 TABLET, FILM COATED in 1 BOTTLE (71335-0598-3) 71335-0598-4 10 TABLET, FILM COATED in 1 BOTTLE (71335-0598-4) 71335-0598-5 120 TABLET, FILM COATED in 1 BOTTLE (71335-0598-5) 71335-0598-6 100 TABLET, FILM COATED in 1 BOTTLE (71335-0598-6)

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": "1cede81a-b1b6-4a31-bba8-9f7d483d2292", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["9a891ab1-675f-498e-a21e-05964307d2dd"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0598-1)", "package_ndc": "71335-0598-1", "marketing_start_date": "20171121"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0598-2)", "package_ndc": "71335-0598-2", "marketing_start_date": "20171121"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0598-3)", "package_ndc": "71335-0598-3", "marketing_start_date": "20171121"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (71335-0598-4)", "package_ndc": "71335-0598-4", "marketing_start_date": "20171121"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (71335-0598-5)", "package_ndc": "71335-0598-5", "marketing_start_date": "20171121"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0598-6)", "package_ndc": "71335-0598-6", "marketing_start_date": "20171121"}], "brand_name": "Eszopiclone", "product_id": "71335-0598_1cede81a-b1b6-4a31-bba8-9f7d483d2292", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71335-0598", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Bryant Ranch Prepack", "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": "20150131", "listing_expiration_date": "20261231"}