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Famotidine

NDC 71335-2527, Famotidine, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-2527
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-2527 \
  -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
71335-2527-17133525270130 TABLET, FILM COATED in 1 BOTTLE (71335-2527-1)
71335-2527-27133525270260 TABLET, FILM COATED in 1 BOTTLE (71335-2527-2)
71335-2527-371335252703100 TABLET, FILM COATED in 1 BOTTLE (71335-2527-3)
71335-2527-47133525270490 TABLET, FILM COATED in 1 BOTTLE (71335-2527-4)
71335-2527-57133525270515 TABLET, FILM COATED in 1 BOTTLE (71335-2527-5)
71335-2527-671335252706120 TABLET, FILM COATED in 1 BOTTLE (71335-2527-6)
71335-2527-77133525270720 TABLET, FILM COATED in 1 BOTTLE (71335-2527-7)
71335-2527-87133525270810 TABLET, FILM COATED in 1 BOTTLE (71335-2527-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e034546b-28cb-41aa-9441-655cdb966554

Use it

Look up 71335-2527 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2527 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2527. 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.