Skip to content
healthcare.dev

Famotidine

NDC 71335-0370, Famotidine, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-0370
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-0370 \
  -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
71335-0370-17133503700130 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)
71335-0370-27133503700260 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)
71335-0370-37133503700320 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)
71335-0370-47133503700490 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)
71335-0370-571335037005100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
71335-0370-67133503700610 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
71335-0370-771335037007120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
71335-0370-87133503700850 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/11ce2a78-76ce-44df-afe3-57493498e596

Use it

Look up 71335-0370 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0370 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0370. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.