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Famotidine

NDC 71205-257, Famotidine, tablet, from Proficient Rx LP.

Product NDC
71205-257
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-257 \
  -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
71205-257-307120502573030 TABLET in 1 BOTTLE (71205-257-30)
71205-257-607120502576060 TABLET in 1 BOTTLE (71205-257-60)
71205-257-907120502579090 TABLET in 1 BOTTLE (71205-257-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1e2003d4-09a3-4cc8-af3d-93d29b9123c0

Use it

Look up 71205-257 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-257 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-257. 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.