Package 68788-7169-2
Brand: eszopiclone
Generic: eszopiclonePackage Facts
Identity
Package NDC
68788-7169-2
Digits Only
6878871692
Product NDC
68788-7169
Description
20 TABLET, FILM COATED in 1 BOTTLE (68788-7169-2)
Marketing
Marketing Status
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": "99eafec4-1437-4b07-ac52-9bd24db7aa9f", "openfda": {"unii": ["UZX80K71OE"], "rxcui": ["485465"], "spl_set_id": ["2b5b4fbb-9b86-46c6-9508-37d3d9806dec"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (68788-7169-1)", "package_ndc": "68788-7169-1", "marketing_start_date": "20180611"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (68788-7169-2)", "package_ndc": "68788-7169-2", "marketing_start_date": "20180611"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68788-7169-3)", "package_ndc": "68788-7169-3", "marketing_start_date": "20180611"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68788-7169-6)", "package_ndc": "68788-7169-6", "marketing_start_date": "20180611"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68788-7169-9)", "package_ndc": "68788-7169-9", "marketing_start_date": "20180611"}], "brand_name": "Eszopiclone", "product_id": "68788-7169_99eafec4-1437-4b07-ac52-9bd24db7aa9f", "dosage_form": "TABLET, FILM COATED", "product_ndc": "68788-7169", "dea_schedule": "CIV", "generic_name": "Eszopiclone", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Eszopiclone", "active_ingredients": [{"name": "ESZOPICLONE", "strength": "3 mg/1"}], "application_number": "ANDA202929", "marketing_category": "ANDA", "marketing_start_date": "20180611", "listing_expiration_date": "20261231"}