escitalopram oxalate

Generic: escitalopram

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name escitalopram oxalate
Generic Name escitalopram
Labeler amneal pharmaceuticals llc
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

escitalopram oxalate 5 mg/5mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 65162-705
Product ID 65162-705_d29f980a-e696-4020-8bf9-8f81016c0699
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202227
Listing Expiration 2026-12-31
Marketing Start 2011-09-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 65162705
Hyphenated Format 65162-705

Supplemental Identifiers

RxCUI
351285
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 ANDA202227 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/5mL
source: ndc
Packaging
  • 240 mL in 1 BOTTLE (65162-705-88)
source: ndc

Packages (1)

65162-705-88 240 mL in 1 BOTTLE (65162-705-88)

Ingredients (1)

escitalopram oxalate (5 mg/5mL)

Linked Drug Pages (1)

Escitalopram Oxalate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d29f980a-e696-4020-8bf9-8f81016c0699", "openfda": {"unii": ["5U85DBW7LO"], "rxcui": ["351285"], "spl_set_id": ["09894a38-4e3a-475d-96cd-c6c8ed87869a"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "240 mL in 1 BOTTLE (65162-705-88)", "package_ndc": "65162-705-88", "marketing_start_date": "20110903"}], "brand_name": "Escitalopram Oxalate", "product_id": "65162-705_d29f980a-e696-4020-8bf9-8f81016c0699", "dosage_form": "SOLUTION", "pharm_class": ["Serotonin Reuptake Inhibitor [EPC]", "Serotonin Uptake Inhibitors [MoA]"], "product_ndc": "65162-705", "generic_name": "Escitalopram", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Escitalopram Oxalate", "active_ingredients": [{"name": "ESCITALOPRAM OXALATE", "strength": "5 mg/5mL"}], "application_number": "ANDA202227", "marketing_category": "ANDA", "marketing_start_date": "20110903", "listing_expiration_date": "20261231"}