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Famotidine

NDC 71205-781, Famotidine, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-781
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075511
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-781 \
  -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
71205-781-307120507813030 TABLET, FILM COATED in 1 BOTTLE (71205-781-30)
71205-781-607120507816060 TABLET, FILM COATED in 1 BOTTLE (71205-781-60)
71205-781-907120507819090 TABLET, FILM COATED in 1 BOTTLE (71205-781-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fe21daca-ac48-4b46-9cb3-9a69af0c6a84

Use it

Look up 71205-781 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-781 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-781. 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.