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Famotidine

NDC 70000-0710, Famotidine, tablet, film coated, from LEADER/ Cardinal Health 110, Inc..

Product NDC
70000-0710
Status
Listed
Labeler
LEADER/ Cardinal Health 110, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA218003
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70000-0710 \
  -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
70000-0710-1700000710011 BOTTLE in 1 CARTON (70000-0710-1) / 200 TABLET, FILM COATED in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 70000071001

    GET /v1/drugs/nadac/70000071001

Use it

Look up 70000-0710 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70000-0710 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70000-0710. 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.