Package 65862-967-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 65862-967-30
Digits Only 6586296730
Product NDC 65862-967
Product ID 65862-967_a39aa520-c8ad-4f39-ad71-04a839474b5b
Description

30 TABLET, FILM COATED in 1 BOTTLE (65862-967-30)

Marketing

Marketing Status
Marketed Since 2016-09-15
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": "a39aa520-c8ad-4f39-ad71-04a839474b5b", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["f18cc76f-82aa-4ad7-b8ce-5737733ee104"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65862-967-01)", "package_ndc": "65862-967-01", "marketing_start_date": "20160915"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-967-30)", "package_ndc": "65862-967-30", "marketing_start_date": "20160915"}], "brand_name": "ESZOPICLONE", "product_id": "65862-967_a39aa520-c8ad-4f39-ad71-04a839474b5b", "dosage_form": "TABLET, FILM COATED", "product_ndc": "65862-967", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}