Package 0456-2005-01

Brand: lexapro

Generic: escitalopram
NDC Package

Package Facts

Identity

Package NDC 0456-2005-01
Digits Only 0456200501
Product NDC 0456-2005
Product ID 0456-2005_9ff46a66-0f97-4a78-9d18-ec576f63bae7
Description

100 TABLET, FILM COATED in 1 BOTTLE (0456-2005-01)

Marketing

Marketing Status
Marketed Since 2002-08-14
Brand lexapro
Generic escitalopram
Sample Package No

Linked Drug Pages (1)

Lexapro ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9ff46a66-0f97-4a78-9d18-ec576f63bae7", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250", "351285", "352272", "352273", "404408", "404420"], "spl_set_id": ["13bb8267-1cab-43e5-acae-55a4d957630a"], "manufacturer_name": ["Allergan, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0456-2005-01)", "package_ndc": "0456-2005-01", "marketing_start_date": "20020814"}], "brand_name": "Lexapro", "product_id": "0456-2005_9ff46a66-0f97-4a78-9d18-ec576f63bae7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0456-2005", "generic_name": "ESCITALOPRAM", "labeler_name": "Allergan, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lexapro", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "NDA021323", "marketing_category": "NDA", "marketing_start_date": "20020814", "listing_expiration_date": "20261231"}