escitalopram oxalate

Generic: escitalopram

Labeler: legacy pharmaceutical packaging, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram
Labeler legacy pharmaceutical packaging, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

escitalopram oxalate 20 mg/1

Manufacturer
Legacy Pharmaceutical Packaging, LLC

Identifiers & Regulatory

Product NDC 68645-520
Product ID 68645-520_2c28cb5c-e64b-9aae-e063-6394a90a9720
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078604
Listing Expiration 2026-12-31
Marketing Start 2016-06-16

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 68645520
Hyphenated Format 68645-520

Supplemental Identifiers

RxCUI
349332 351250
UPC
0368645519548 0368645520544
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 oxalate (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number ANDA078604 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54)
source: ndc

Packages (1)

68645-520-54 30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54)

Ingredients (1)

escitalopram oxalate (20 mg/1)

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c28cb5c-e64b-9aae-e063-6394a90a9720", "openfda": {"upc": ["0368645519548", "0368645520544"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351250"], "spl_set_id": ["9c68f89b-1d34-4735-9631-817f012935d7"], "manufacturer_name": ["Legacy Pharmaceutical Packaging, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68645-520-54)", "package_ndc": "68645-520-54", "marketing_start_date": "20160616"}], "brand_name": "Escitalopram Oxalate", "product_id": "68645-520_2c28cb5c-e64b-9aae-e063-6394a90a9720", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "68645-520", "generic_name": "Escitalopram", "labeler_name": "Legacy Pharmaceutical Packaging, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "20 mg/1"}], "application_number": "ANDA078604", "marketing_category": "ANDA", "marketing_start_date": "20160616", "listing_expiration_date": "20261231"}