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Famotidine

NDC 61442-121, Famotidine, tablet, from Carlsbad Technology, Inc.

Product NDC
61442-121
Status
Listed
Labeler
Carlsbad Technology, Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/61442-121 \
  -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
61442-121-016144201210124 BOTTLE in 1 BOX (61442-121-01) / 100 TABLET in 1 BOTTLE
61442-121-056144201210524 BOTTLE in 1 BOX (61442-121-05) / 500 TABLET in 1 BOTTLE
61442-121-106144201211012 BOTTLE in 1 BOX (61442-121-10) / 1000 TABLET in 1 BOTTLE
61442-121-306144201213024 BOTTLE in 1 BOX (61442-121-30) / 30 TABLET in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a8b5c855-053d-4295-8f57-1a96a6ccaa92

  • NADAC price for package 61442012101

    GET /v1/drugs/nadac/61442012101

  • NADAC price for package 61442012110

    GET /v1/drugs/nadac/61442012110

Use it

Look up 61442-121 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61442-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61442-121. 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.