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Famotidine

NDC 51655-233, Famotidine, tablet, film coated, from Northwind Health Company, LLC.

Product NDC
51655-233
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075511
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
51655-233-255165502332560 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-25)
51655-233-265165502332690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-26)
51655-233-525165502335230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-233-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2b6da72-72ea-d81b-e053-2995a90a9526

Use it

Look up 51655-233 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-233 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-233. 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.