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FAMOTIDINE

NDC 72865-214, Famotidine, tablet, film coated, from XLCare Pharmaceuticals, Inc..

Product NDC
72865-214
Status
Listed
Labeler
XLCare Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215689
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-214 \
  -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
72865-214-0172865021401100 TABLET, FILM COATED in 1 BOTTLE (72865-214-01)
72865-214-0572865021405500 TABLET, FILM COATED in 1 BOTTLE (72865-214-05)
72865-214-1872865021418180 TABLET, FILM COATED in 1 BOTTLE (72865-214-18)
72865-214-307286502143030 TABLET, FILM COATED in 1 BOTTLE (72865-214-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7b550cf9-221f-4f28-ba99-414ad7d5612f

Use it

Look up 72865-214 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-214 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-214. 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.