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Famotidine

NDC 85766-222, Famotidine, tablet, film coated, from Sportpharm LLC.

Product NDC
85766-222
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/85766-222 \
  -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
85766-222-0185766022201100 TABLET, FILM COATED in 1 BOTTLE (85766-222-01)
85766-222-07857660222077 TABLET, FILM COATED in 1 BOTTLE (85766-222-07)
85766-222-108576602221010 TABLET, FILM COATED in 1 BOTTLE (85766-222-10)
85766-222-148576602221414 TABLET, FILM COATED in 1 BOTTLE (85766-222-14)
85766-222-158576602221515 TABLET, FILM COATED in 1 BOTTLE (85766-222-15)
85766-222-208576602222020 TABLET, FILM COATED in 1 BOTTLE (85766-222-20)
85766-222-308576602223030 TABLET, FILM COATED in 1 BOTTLE (85766-222-30)
85766-222-608576602226060 TABLET, FILM COATED in 1 BOTTLE (85766-222-60)
85766-222-908576602229090 TABLET, FILM COATED in 1 BOTTLE (85766-222-90)

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 85766-222 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85766-222 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85766-222. 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.