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Citalopram

NDC 51655-664, Citalopram, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-664
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078216
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-664 \
  -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
51655-664-255165506642560 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-664-25)
51655-664-265165506642690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-664-26)
51655-664-525165506645230 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-664-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a7ef6ad2-5f22-4ac7-b57a-f498bcb53be1

Use it

Look up 51655-664 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-664 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-664. 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.