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Famotidine

NDC 10267-5690, Famotidine, tablet, coated, from Contract Pharmacal Corp..

Product NDC
10267-5690
Status
Listed
Labeler
Contract Pharmacal Corp.
Dosage form
TABLET, COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217669
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/10267-5690 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
10267-5690-110267569001100 TABLET, COATED in 1 BOTTLE (10267-5690-1)
10267-5690-4102675690041000 TABLET, COATED in 1 BOTTLE (10267-5690-4)
10267-5690-510267569005500 TABLET, COATED in 1 BOTTLE (10267-5690-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/273deac8-c2b0-423f-8662-4f16d91df216

Use it

Look up 10267-5690 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/10267-5690 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 10267-5690. 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.