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Famotidine

NDC 50383-913, Famotidine, powder, for solution, from Akorn.

Product NDC
50383-913
Status
Listed
Labeler
Akorn
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201995
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50383-913 \
  -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
50383-913-40503830913401 BOTTLE, GLASS in 1 CARTON (50383-913-40) / 50 mL in 1 BOTTLE, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/354a5a02-45cb-4ab0-88ee-6635d5a43b01

Use it

Look up 50383-913 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50383-913 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50383-913. 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.