escitalopram
Generic: escitalopram
Labeler: almatica pharma llcDrug Facts
Product Profile
Brand Name
escitalopram
Generic Name
escitalopram
Labeler
almatica pharma llc
Dosage Form
CAPSULE
Routes
Active Ingredients
escitalopram oxalate 15 mg/1
Manufacturer
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
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
52427795
Hyphenated Format
52427-795
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 15 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (52427-795-30)
Packages (1)
Ingredients (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"}