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Famotidine

NDC 27241-249, Famotidine, for suspension, from Ajanta Pharma USA Inc..

Product NDC
27241-249
Status
Listed
Labeler
Ajanta Pharma USA Inc.
Dosage form
FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217529
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/27241-249 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
27241-249-492724102494950 mL in 1 BOTTLE (27241-249-49)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a88e7069-230c-4105-ade0-a98968e18671

  • NADAC price for package 27241024949

    GET /v1/drugs/nadac/27241024949

Use it

Look up 27241-249 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/27241-249 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 27241-249. 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.