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Famotidine

NDC 55111-120, Famotidine, tablet, film coated, from Dr.Reddy's Laboratories Limited.

Product NDC
55111-120
Status
Listed
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075718
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-120 \
  -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
55111-120-0155111012001100 TABLET, FILM COATED in 1 BOTTLE (55111-120-01)
55111-120-10551110120101000 TABLET, FILM COATED in 1 BOTTLE (55111-120-10)
55111-120-305511101203030 TABLET, FILM COATED in 1 BOTTLE (55111-120-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06d286ce-14b3-4b66-8b42-ac4a10a0fc90

Use it

Look up 55111-120 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-120 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-120. 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.