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Famotidine

NDC 60760-937, Famotidine, tablet, film coated, from ST. MARY'S MEDICAL PARK PHARMACY.

Product NDC
60760-937
Status
Listed
Labeler
ST. MARY'S MEDICAL PARK PHARMACY
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/60760-937 \
  -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
60760-937-07607600937077 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-937-07)
60760-937-606076009376060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-937-60)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/31cdc900-fe17-2d5f-e063-6294a90a0fda

Use it

Look up 60760-937 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60760-937 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60760-937. 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.