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Famotidine

NDC 68001-398, Famotidine, tablet, film coated, from BluePoint Laboratories.

Product NDC
68001-398
Status
Listed
Labeler
BluePoint Laboratories
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/68001-398 \
  -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
68001-398-0068001039800100 TABLET, FILM COATED in 1 BOTTLE (68001-398-00)
68001-398-0368001039803500 TABLET, FILM COATED in 1 BOTTLE (68001-398-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8c7ca3cc-ff90-42a7-9218-554cf15348a3

  • NADAC price for package 68001039800

    GET /v1/drugs/nadac/68001039800

  • NADAC price for package 68001039803

    GET /v1/drugs/nadac/68001039803

Use it

Look up 68001-398 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-398 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-398. 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.