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Famotidine

NDC 71205-535, Famotidine, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-535
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206530
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-535 \
  -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
71205-535-06712050535066 TABLET, FILM COATED in 1 BOTTLE (71205-535-06)
71205-535-107120505351010 TABLET, FILM COATED in 1 BOTTLE (71205-535-10)
71205-535-307120505353030 TABLET, FILM COATED in 1 BOTTLE (71205-535-30)
71205-535-607120505356060 TABLET, FILM COATED in 1 BOTTLE (71205-535-60)
71205-535-7871205053578180 TABLET, FILM COATED in 1 BOTTLE (71205-535-78)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4adb4864-04ac-4cb1-96c2-6196a30ac640

Use it

Look up 71205-535 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-535 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-535. 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.