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Famotidine

NDC 68001-494, Famotidine, tablet, from BluePoint Laboratories.

Product NDC
68001-494
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA206531
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-494 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
68001-494-04680010494041 BOTTLE in 1 CARTON (68001-494-04) / 30 TABLET in 1 BOTTLE
68001-494-06680010494061 BOTTLE in 1 CARTON (68001-494-06) / 60 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 68001049404

    GET /v1/drugs/nadac/68001049404

  • NADAC price for package 68001049406

    GET /v1/drugs/nadac/68001049406

Use it

Look up 68001-494 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-494 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-494. 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.