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Famotidine

NDC 80425-0589, Famotidine, tablet, film coated, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0589
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217400
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0589 \
  -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
80425-0589-18042505890130 TABLET, FILM COATED in 1 BOTTLE (80425-0589-1)
80425-0589-28042505890260 TABLET, FILM COATED in 1 BOTTLE (80425-0589-2)
80425-0589-38042505890390 TABLET, FILM COATED in 1 BOTTLE (80425-0589-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5648ca13-1add-56ec-e063-6294a90a6f29

Use it

Look up 80425-0589 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0589 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0589. 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.