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famotidine

NDC 83324-003, famotidine, tablet, film coated, from CHAIN DRUG MARKETING ASSOCIATION, INC..

Product NDC
83324-003
Status
Listed
Labeler
CHAIN DRUG MARKETING ASSOCIATION, INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215766
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/83324-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
83324-003-30833240003301 CONTAINER in 1 CARTON (83324-003-30) / 30 TABLET, FILM COATED in 1 CONTAINER

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 83324-003 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/83324-003 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 83324-003. 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.