Package 0093-5537-56

Brand: eszopiclone

Generic: eszopiclone
NDC Package

Package Facts

Identity

Package NDC 0093-5537-56
Digits Only 0093553756
Product NDC 0093-5537
Product ID 0093-5537_efcf4106-ac0a-4f8b-bcd0-743e45e66924
Description

30 TABLET, FILM COATED in 1 BOTTLE (0093-5537-56)

Marketing

Marketing Status
Discontinued 2027-01-31
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": "efcf4106-ac0a-4f8b-bcd0-743e45e66924", "openfda": {"upc": ["0300935538013", "0300935539010", "0300935537566"], "unii": ["UZX80K71OE"], "rxcui": ["485440", "485442", "485465"], "spl_set_id": ["2435e2f1-bc52-488f-80e9-f1758e354aae"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-5537-56)", "package_ndc": "0093-5537-56", "marketing_end_date": "20270131", "marketing_start_date": "20140414"}], "brand_name": "Eszopiclone", "product_id": "0093-5537_efcf4106-ac0a-4f8b-bcd0-743e45e66924", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0093-5537", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "1 mg/1"}], "application_number": "ANDA091169", "marketing_category": "ANDA", "marketing_end_date": "20270131", "marketing_start_date": "20140414"}