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Famotidine

NDC 43386-500, Famotidine, for suspension, from Lupin Pharmaceuticals,Inc..

Product NDC
43386-500
Status
Listed
Labeler
Lupin Pharmaceuticals,Inc.
Dosage form
FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201695
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43386-500 \
  -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
43386-500-114338605001150 mL in 1 BOTTLE (43386-500-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a0bdf4d1-8458-4e4f-95aa-bcc38c0f32f8

Use it

Look up 43386-500 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43386-500 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43386-500. 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.