eszopiclone

Generic: eszopiclone

Labeler: lupin pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

eszopiclone 1 mg/1

Manufacturer
Lupin Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68180-322
Product ID 68180-322_a3530781-6fea-425f-9958-eeb2d0b3c696
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091124
DEA Schedule civ
Listing Expiration 2026-12-31
Marketing Start 2014-04-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68180322
Hyphenated Format 68180-322

Supplemental Identifiers

RxCUI
485440 485442 485465
UPC
0368180324010 0368180323013 0368180322016
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 ANDA091124 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)
source: ndc

Packages (1)

68180-322-01 100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)

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": "a3530781-6fea-425f-9958-eeb2d0b3c696", "openfda": {"upc": ["0368180324010", "0368180323013", "0368180322016"], "unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["7068c455-691e-4c56-9857-b7b4e13f4784"], "manufacturer_name": ["Lupin Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68180-322-01)", "package_ndc": "68180-322-01", "marketing_start_date": "20140415"}], "brand_name": "Eszopiclone", "product_id": "68180-322_a3530781-6fea-425f-9958-eeb2d0b3c696", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68180-322", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Lupin Pharmaceuticals, Inc.", "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": "20140415", "listing_expiration_date": "20261231"}