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Famotidine

NDC 71335-0231, Famotidine, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0231
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0231 \
  -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
71335-0231-17133502310130 TABLET in 1 BOTTLE (71335-0231-1)
71335-0231-27133502310260 TABLET in 1 BOTTLE (71335-0231-2)
71335-0231-371335023103100 TABLET in 1 BOTTLE (71335-0231-3)
71335-0231-47133502310490 TABLET in 1 BOTTLE (71335-0231-4)
71335-0231-57133502310515 TABLET in 1 BOTTLE (71335-0231-5)
71335-0231-671335023106120 TABLET in 1 BOTTLE (71335-0231-6)
71335-0231-77133502310720 TABLET in 1 BOTTLE (71335-0231-7)
71335-0231-87133502310810 TABLET in 1 BOTTLE (71335-0231-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/db3af7cc-efc6-4934-acff-8bb2d31fe829

Use it

Look up 71335-0231 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0231 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0231. 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.