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Famotidine

NDC 69238-2090, Famotidine, powder, for suspension, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-2090
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216427
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2090 \
  -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
69238-2090-46923820900450 mL in 1 BOTTLE (69238-2090-4)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/bb602b05-0ce6-4029-bd6e-291076e64efb

  • NADAC price for package 69238209004

    GET /v1/drugs/nadac/69238209004

Use it

Look up 69238-2090 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2090 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-2090. 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.