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FAMOTIDINE

NDC 67877-843, FAMOTIDINE, tablet, film coated, from Ascend Laboratories, LLC.

Product NDC
67877-843
Status
Listed
Labeler
Ascend Laboratories, LLC
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/67877-843 \
  -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
67877-843-0167877084301100 TABLET, FILM COATED in 1 BOTTLE (67877-843-01)
67877-843-0567877084305500 TABLET, FILM COATED in 1 BOTTLE (67877-843-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ea50552f-f9b9-467f-a925-62ff027df607

  • NADAC price for package 67877084301

    GET /v1/drugs/nadac/67877084301

  • NADAC price for package 67877084305

    GET /v1/drugs/nadac/67877084305

Use it

Look up 67877-843 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-843 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-843. 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.