Package 0615-8477-39

Brand: escitalopram

Generic: escitalopram oxalate
NDC Package

Package Facts

Identity

Package NDC 0615-8477-39
Digits Only 0615847739
Product NDC 0615-8477
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-39)

Marketing

Marketing Status
Marketed Since 2023-07-18
Brand escitalopram
Generic escitalopram oxalate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "356b8a10-241f-41e7-96fe-57590f373800", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351250"], "spl_set_id": ["ac9ede0c-7912-4e7d-83b3-964feee61215"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-05)", "package_ndc": "0615-8477-05", "marketing_start_date": "20230718"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8477-39)", "package_ndc": "0615-8477-39", "marketing_start_date": "20230718"}], "brand_name": "Escitalopram", "product_id": "0615-8477_356b8a10-241f-41e7-96fe-57590f373800", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "0615-8477", "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": "20 mg/1"}], "application_number": "ANDA090432", "marketing_category": "ANDA", "marketing_start_date": "20120911", "listing_expiration_date": "20261231"}