escitalopram

Generic: escitalopram

Labeler: macleods pharmaceuticals limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram
Generic Name escitalopram
Labeler macleods pharmaceuticals limited
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

escitalopram oxalate 5 mg/5mL

Manufacturer
Macleods Pharmaceuticals Limited

Identifiers & Regulatory

Product NDC 33342-053
Product ID 33342-053_6dea1a7d-7262-4d3e-9c9e-1db9c8587066
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202754
Listing Expiration 2026-12-31
Marketing Start 2016-03-31

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 33342053
Hyphenated Format 33342-053

Supplemental Identifiers

RxCUI
351285
UPC
0333342053282
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 ANDA202754 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 240 mL in 1 BOTTLE (33342-053-28)
source: ndc

Packages (1)

33342-053-28 240 mL in 1 BOTTLE (33342-053-28)

Ingredients (1)

escitalopram oxalate (5 mg/5mL)

Linked Drug Pages (1)

escitalopram ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6dea1a7d-7262-4d3e-9c9e-1db9c8587066", "openfda": {"upc": ["0333342053282"], "unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["4d5c3142-b850-49b9-9f5c-81fe15ea7bfb"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (33342-053-28)", "package_ndc": "33342-053-28", "marketing_start_date": "20160331"}], "brand_name": "escitalopram", "product_id": "33342-053_6dea1a7d-7262-4d3e-9c9e-1db9c8587066", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "33342-053", "generic_name": "escitalopram", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "escitalopram", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA202754", "marketing_category": "ANDA", "marketing_start_date": "20160331", "listing_expiration_date": "20261231"}