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Famotidine

NDC 21130-023, Famotidine, tablet, from Albertsons Companies.

Product NDC
21130-023
Status
Listed
Labeler
Albertsons Companies
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA077367
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/21130-023 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
21130-023-25211300023251 BOTTLE in 1 CARTON (21130-023-25) / 25 TABLET in 1 BOTTLE

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 21130-023 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/21130-023 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 21130-023. 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.