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FAMOTIDINE

NDC 81033-023, FAMOTIDINE, powder, for suspension, from Kesin Pharma Corporation.

Product NDC
81033-023
Status
Listed
Labeler
Kesin Pharma Corporation
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217137
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/81033-023 \
  -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
81033-023-508103300235050 mL in 1 BOTTLE (81033-023-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/446ca466-a43c-0401-e063-6394a90ac0d1

  • NADAC price for package 81033002350

    GET /v1/drugs/nadac/81033002350

Use it

Look up 81033-023 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81033-023 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81033-023. 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.