Skip to content
healthcare.dev

Famotidine

NDC 71821-010, Famotidine, tablet, film coated, from VKT Pharma Private Limited.

Product NDC
71821-010
Status
Listed
Labeler
VKT Pharma Private Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA215822
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71821-010 \
  -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
71821-010-1271821001012144230 TABLET, FILM COATED in 1 BAG (71821-010-12)
71821-010-1371821001013144230 TABLET, FILM COATED in 1 BAG (71821-010-13)

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 71821-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71821-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71821-010. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.