Package 71205-236-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 71205-236-30
Digits Only 7120523630
Product NDC 71205-236
Product ID 71205-236_257152f7-f81c-4be1-89ab-6ec7044555ff
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-236-30)

Marketing

Marketing Status
Marketed Since 2019-03-01
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": "257152f7-f81c-4be1-89ab-6ec7044555ff", "openfda": {"upc": ["0371205236304"], "unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["2f4fa6e8-be82-4fb5-9a11-9ba8f557c027"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-236-30)", "package_ndc": "71205-236-30", "marketing_start_date": "20190301"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-236-60)", "package_ndc": "71205-236-60", "marketing_start_date": "20190301"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-236-90)", "package_ndc": "71205-236-90", "marketing_start_date": "20190301"}], "brand_name": "ESZOPICLONE", "product_id": "71205-236_257152f7-f81c-4be1-89ab-6ec7044555ff", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71205-236", "dea_schedule": "CIV", "generic_name": "ESZOPICLONE", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESZOPICLONE", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}