escitalopram

Generic: escitalopram oxalate

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram oxalate
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 10 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8476
Product ID 0615-8476_efdc3d31-555b-443b-bdc7-4729675ab6c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090432
Listing Expiration 2026-12-31
Marketing Start 2012-09-11

Pharmacologic Class

Classes
serotonin reuptake inhibitor [epc] serotonin uptake inhibitors [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158476
Hyphenated Format 0615-8476

Supplemental Identifiers

RxCUI
349332 351249
UNII
5U85DBW7LO

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name escitalopram (source: ndc)
Generic Name escitalopram oxalate (source: ndc)
Application Number ANDA090432 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-05)
  • 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28)
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-39)
source: ndc

Packages (3)

0615-8476-05 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-05) 0615-8476-28 28 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-28) 0615-8476-39 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8476-39)

Ingredients (1)

escitalopram oxalate (10 mg/1)

Linked Drug Pages (1)

Escitalopram ndc-match (0.9)

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"}