Package 68180-322-01

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 68180-322-01
Digits Only 6818032201
Product NDC 68180-322
Product ID 68180-322_a3530781-6fea-425f-9958-eeb2d0b3c696
Description

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

Marketing

Marketing Status
Marketed Since 2014-04-15
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (1)

Eszopiclone ndc-match (0.95)

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"}