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Famotidine

NDC 82868-077, Famotidine, tablet, from Northwind Health Company, LLC.

Product NDC
82868-077
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82868-077 \
  -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
82868-077-308286800773030 TABLET in 1 BOTTLE, PLASTIC (82868-077-30)
82868-077-608286800776060 TABLET in 1 BOTTLE, PLASTIC (82868-077-60)
82868-077-908286800779090 TABLET in 1 BOTTLE, PLASTIC (82868-077-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/43454e0f-4e1e-bbc6-e063-6394a90a5ac4

Use it

Look up 82868-077 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82868-077 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82868-077. 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.