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Famotidine

NDC 68001-397, Famotidine, tablet, film coated, from BluePoint Laboratories.

Product NDC
68001-397
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/68001-397 \
  -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
68001-397-0068001039700100 TABLET, FILM COATED in 1 BOTTLE (68001-397-00)
68001-397-08680010397081000 TABLET, FILM COATED in 1 BOTTLE (68001-397-08)

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 68001039700

    GET /v1/drugs/nadac/68001039700
  • NADAC price for package 68001039708

    GET /v1/drugs/nadac/68001039708

Use it

Look up 68001-397 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-397 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-397. 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.