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Famotidine

NDC 72603-171, Famotidine, powder, for suspension, from NorthStar Rx LLC.

Product NDC
72603-171
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215043
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72603-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
72603-171-017260301710150 mL in 1 BOTTLE (72603-171-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/04aaf296-f136-29d7-e063-6294a90affe1

  • NADAC price for package 72603017101

    GET /v1/drugs/nadac/72603017101

Use it

Look up 72603-171 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72603-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72603-171. 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.