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Famotidine

NDC 50268-299, Famotidine, tablet, film coated, from AvPAK.

Product NDC
50268-299
Status
Listed
Labeler
AvPAK
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075718
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-299 \
  -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
50268-299-155026802991550 BLISTER PACK in 1 BOX (50268-299-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-299-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dfdca61d-8824-6230-e053-2995a90a209d

  • NADAC price for package 50268029915

    GET /v1/drugs/nadac/50268029915

Use it

Look up 50268-299 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-299 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-299. 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.