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Escitalopram Oxalate

NDC 65162-021, Escitalopram Oxalate, tablet, film coated, from Amneal Pharmaceuticals LLC.

Product NDC
65162-021
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205619
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-021 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • ESCITALOPRAM OXALATE20 mg/1

Pharmacologic classes

Serotonin Reuptake Inhibitor [EPC]; Serotonin Uptake Inhibitors [MoA]

Package NDCNDC-11Package
65162-021-036516200210330 TABLET, FILM COATED in 1 BOTTLE (65162-021-03)
65162-021-096516200210990 TABLET, FILM COATED in 1 BOTTLE (65162-021-09)
65162-021-11651620021111000 TABLET, FILM COATED in 1 BOTTLE (65162-021-11)
65162-021-5065162002150500 TABLET, FILM COATED in 1 BOTTLE (65162-021-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8704d062-fa91-4224-9dec-41664d20ee6b

Use it

Look up 65162-021 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-021 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-021. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.