eszopiclone

Generic: eszopiclone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name eszopiclone
Generic Name eszopiclone
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

eszopiclone 2 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-7745
Product ID 50090-7745_8d97a3fa-9561-4691-b516-5e78c2f9c875
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208451
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2016-09-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500907745
Hyphenated Format 50090-7745

Supplemental Identifiers

RxCUI
485442
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 ANDA208451 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-7745-0)
source: ndc

Packages (1)

50090-7745-0 30 TABLET, FILM COATED in 1 BOTTLE (50090-7745-0)

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": "8d97a3fa-9561-4691-b516-5e78c2f9c875", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485442"], "spl_set_id": ["923cc646-f22a-4a26-88f7-a19fce016321"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-7745-0)", "package_ndc": "50090-7745-0", "marketing_start_date": "20251030"}], "brand_name": "ESZOPICLONE", "product_id": "50090-7745_8d97a3fa-9561-4691-b516-5e78c2f9c875", "dosage_form": "TABLET, FILM COATED", "product_ndc": "50090-7745", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "2 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}