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FAMOTIDINE

NDC 85534-0092, FAMOTIDINE, tablet, film coated, from HAWAII REPACK, INC..

Product NDC
85534-0092
Status
Listed
Labeler
HAWAII REPACK, INC.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215630
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0092 \
  -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
85534-0092-08553400920030 TABLET, FILM COATED in 1 BOTTLE (85534-0092-0)
85534-0092-18553400920160 TABLET, FILM COATED in 1 BOTTLE (85534-0092-1)
85534-0092-28553400920290 TABLET, FILM COATED in 1 BOTTLE (85534-0092-2)
85534-0092-385534009203120 TABLET, FILM COATED in 1 BOTTLE (85534-0092-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/eec89230-47fc-4139-a370-b4f9e225e8c0

Use it

Look up 85534-0092 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/85534-0092 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 85534-0092. 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.