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Citalopram

NDC 51655-137, Citalopram, tablet, from Northwind Health Company, LLC.

Product NDC
51655-137
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077534
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-137 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CITALOPRAM HYDROBROMIDE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-137-265165501372690 TABLET in 1 BOTTLE, PLASTIC (51655-137-26)
51655-137-525165501375230 TABLET in 1 BOTTLE, PLASTIC (51655-137-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2b42bdc-47e0-19c5-e053-2a95a90a1828

Use it

Look up 51655-137 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-137 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-137. 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.