escitalopram

Generic: escitalopram

Labeler: almatica pharma llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler almatica pharma llc
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

escitalopram oxalate 15 mg/1

Manufacturer
Almatica Pharma LLC

Identifiers & Regulatory

Product NDC 52427-795
Product ID 52427-795_4caf6d36-950a-522b-5914-079783778c6f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA219130
Listing Expiration 2026-12-31
Marketing Start 2025-10-06

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 52427795
Hyphenated Format 52427-795

Supplemental Identifiers

RxCUI
2725159
UPC
0352427795305
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 (source: ndc)
Generic Name escitalopram (source: ndc)
Application Number NDA219130 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 15 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (52427-795-30)
source: ndc

Packages (1)

Ingredients (1)

escitalopram oxalate (15 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4caf6d36-950a-522b-5914-079783778c6f", "openfda": {"upc": ["0352427795305"], "unii": ["5U85DBW7LO"], "rxcui": ["2725159"], "spl_set_id": ["c0401570-a3b0-bef2-7365-c23dc952b8b6"], "manufacturer_name": ["Almatica Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (52427-795-30)", "package_ndc": "52427-795-30", "marketing_start_date": "20251006"}], "brand_name": "escitalopram", "product_id": "52427-795_4caf6d36-950a-522b-5914-079783778c6f", "dosage_form": "CAPSULE", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "52427-795", "generic_name": "escitalopram", "labeler_name": "Almatica Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "15 mg/1"}], "application_number": "NDA219130", "marketing_category": "NDA", "marketing_start_date": "20251006", "listing_expiration_date": "20261231"}