Package 0615-8476-28

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 0615-8476-28
Digits Only 0615847628
Product NDC 0615-8476
Product ID 0615-8476_efdc3d31-555b-443b-bdc7-4729675ab6c1
Description

28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28)

Marketing

Marketing Status
Marketed Since 2025-01-15
Brand escitalopram
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Escitalopram ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "efdc3d31-555b-443b-bdc7-4729675ab6c1", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249"], "spl_set_id": ["b29ae169-d60b-464a-9763-f1d8d9e0598d"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-05)", "package_ndc": "0615-8476-05", "marketing_start_date": "20230510"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28)", "package_ndc": "0615-8476-28", "marketing_start_date": "20250115"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-39)", "package_ndc": "0615-8476-39", "marketing_start_date": "20230510"}], "brand_name": "Escitalopram", "product_id": "0615-8476_efdc3d31-555b-443b-bdc7-4729675ab6c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8476", "generic_name": "Escitalopram Oxalate", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "10 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}