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Famotidine

NDC 85766-221, Famotidine, tablet, film coated, from Sportpharm LLC.

Product NDC
85766-221
Status
Listed
Labeler
Sportpharm LLC
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/85766-221 \
  -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
85766-221-0185766022101100 TABLET, FILM COATED in 1 BOTTLE (85766-221-01)
85766-221-07857660221077 TABLET, FILM COATED in 1 BOTTLE (85766-221-07)
85766-221-108576602211010 TABLET, FILM COATED in 1 BOTTLE (85766-221-10)
85766-221-148576602211414 TABLET, FILM COATED in 1 BOTTLE (85766-221-14)
85766-221-158576602211515 TABLET, FILM COATED in 1 BOTTLE (85766-221-15)
85766-221-208576602212020 TABLET, FILM COATED in 1 BOTTLE (85766-221-20)
85766-221-308576602213030 TABLET, FILM COATED in 1 BOTTLE (85766-221-30)
85766-221-608576602216060 TABLET, FILM COATED in 1 BOTTLE (85766-221-60)
85766-221-908576602219090 TABLET, FILM COATED in 1 BOTTLE (85766-221-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4421ceb7-a114-436c-871a-7bc5444f8154

Use it

Look up 85766-221 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85766-221 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85766-221. 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.