escitalopram oxalate

Generic: escitalopram

Labeler: ascent pharmaceuticals, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram
Labeler ascent pharmaceuticals, inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

escitalopram oxalate 5 mg/1

Manufacturer
Ascent Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 43602-473
Product ID 43602-473_c891ea0b-ed9d-4e75-a529-2b8a651034d2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215177
Listing Expiration 2026-12-31
Marketing Start 2025-07-15

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43602473
Hyphenated Format 43602-473

Supplemental Identifiers

RxCUI
349332 351249 351250
UPC
0343602474306 0343602475303 0343602474108 0343602473101 0343602473309
UNII
5U85DBW7LO

Packaging Origin

Original Packager
true

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 ANDA215177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE (43602-473-10)
  • 30 TABLET in 1 BOTTLE (43602-473-30)
source: ndc

Packages (2)

43602-473-10 1000 TABLET in 1 BOTTLE (43602-473-10) 43602-473-30 30 TABLET in 1 BOTTLE (43602-473-30)

Ingredients (1)

escitalopram oxalate (5 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": "c891ea0b-ed9d-4e75-a529-2b8a651034d2", "openfda": {"upc": ["0343602474306", "0343602475303", "0343602474108", "0343602473101", "0343602473309"], "unii": ["5U85DBW7LO"], "rxcui": ["349332", "351249", "351250"], "spl_set_id": ["1285841d-d9f8-49c6-9456-bf51c8e37271"], "manufacturer_name": ["Ascent Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (43602-473-10)", "package_ndc": "43602-473-10", "marketing_start_date": "20250715"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (43602-473-30)", "package_ndc": "43602-473-30", "marketing_start_date": "20250715"}], "brand_name": "ESCITALOPRAM OXALATE", "product_id": "43602-473_c891ea0b-ed9d-4e75-a529-2b8a651034d2", "dosage_form": "TABLET", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "43602-473", "generic_name": "escitalopram", "labeler_name": "Ascent Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ESCITALOPRAM OXALATE", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/1"}], "application_number": "ANDA215177", "marketing_category": "ANDA", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}