Package 71205-384-30

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 71205-384-30
Digits Only 7120538430
Product NDC 71205-384
Description

30 TABLET, FILM COATED in 1 BOTTLE (71205-384-30)

Marketing

Marketing Status
Marketed Since 2020-01-10
Brand eszopiclone
Generic eszopiclone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fe5e114-9285-4448-a98e-24820b998749", "openfda": {"upc": ["0371205384609"], "unii": ["UZX80K71OE"], "rxcui": ["485440"], "spl_set_id": ["024f833e-c20c-46a2-971b-3f2a716b1678"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-384-30)", "package_ndc": "71205-384-30", "marketing_start_date": "20200110"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-384-60)", "package_ndc": "71205-384-60", "marketing_start_date": "20200110"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-384-90)", "package_ndc": "71205-384-90", "marketing_start_date": "20200110"}], "brand_name": "ESZOPICLONE", "product_id": "71205-384_7fe5e114-9285-4448-a98e-24820b998749", "dosage_form": "TABLET, FILM COATED", "product_ndc": "71205-384", "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": "1 mg/1"}], "application_number": "ANDA208451", "marketing_category": "ANDA", "marketing_start_date": "20160915", "listing_expiration_date": "20261231"}