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Famotidine

NDC 0172-5729, Famotidine, tablet, film coated, from Teva Pharmaceuticals USA, Inc..

Product NDC
0172-5729
Status
Listed
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075511
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0172-5729 \
  -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
0172-5729-6000172572960100 TABLET, FILM COATED in 1 BOTTLE (0172-5729-60)
0172-5729-7000172572970500 TABLET, FILM COATED in 1 BOTTLE (0172-5729-70)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4c6f4f9e-f3f5-4ecf-9f40-887e037e8847

  • NADAC price for package 00172572960

    GET /v1/drugs/nadac/00172572960

  • NADAC price for package 00172572970

    GET /v1/drugs/nadac/00172572970

Use it

Look up 0172-5729 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0172-5729 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0172-5729. 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.