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FAMOTIDINE

NDC 42571-433, FAMOTIDINE, powder, for suspension, from Micro Labs Limited.

Product NDC
42571-433
Status
Listed
Labeler
Micro Labs Limited
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217842
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42571-433 \
  -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
42571-433-454257104334550 mL in 1 BOTTLE (42571-433-45)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1756ab7d-05c4-4726-8f72-4e8363440968

  • NADAC price for package 42571043345

    GET /v1/drugs/nadac/42571043345

Use it

Look up 42571-433 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-433 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-433. 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.