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Famotidine

NDC 31722-017, Famotidine, tablet, film coated, from Camber Pharmaceuticals, Inc..

Product NDC
31722-017
Status
Listed
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215767
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/31722-017 \
  -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
31722-017-0131722001701100 TABLET, FILM COATED in 1 BOTTLE (31722-017-01)
31722-017-10317220017101000 TABLET, FILM COATED in 1 BOTTLE (31722-017-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/902b5d4b-1707-4312-9f46-ef5ab86b00f0

  • NADAC price for package 31722001701

    GET /v1/drugs/nadac/31722001701

  • NADAC price for package 31722001710

    GET /v1/drugs/nadac/31722001710

Use it

Look up 31722-017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/31722-017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 31722-017. 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.