Skip to content
healthcare.dev

Famotidine

NDC 69367-401, Famotidine, tablet, coated, from Westminster Pharmaceuticals, LLC.

Product NDC
69367-401
Status
Listed
Labeler
Westminster Pharmaceuticals, LLC
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217669
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69367-401 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
69367-401-10693670401101000 TABLET, COATED in 1 BOTTLE, PLASTIC (69367-401-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c0e15f57-ab20-4030-b1d1-6aff33be7d76
  • NADAC price for package 69367040110

    GET /v1/drugs/nadac/69367040110

Use it

Look up 69367-401 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69367-401 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69367-401. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.