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Famotidine

NDC 43598-572, Famotidine, for suspension, from DR. REDDY'S LABORATORIES INC.

Product NDC
43598-572
Status
Listed
Labeler
DR. REDDY'S LABORATORIES INC
Dosage form
FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217605
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43598-572 \
  -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
43598-572-114359805721150 mL in 1 BOTTLE (43598-572-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/88ac92eb-5684-46c8-8cd2-3d4aefee26cf

Use it

Look up 43598-572 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43598-572 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43598-572. 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.