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FAMOTIDINE

NDC 67877-842, FAMOTIDINE, tablet, film coated, from Ascend Laboratories, LLC.

Product NDC
67877-842
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/67877-842 \
  -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
67877-842-0167877084201100 TABLET, FILM COATED in 1 BOTTLE (67877-842-01)
67877-842-0567877084205500 TABLET, FILM COATED in 1 BOTTLE (67877-842-05)
67877-842-10678770842101000 TABLET, FILM COATED in 1 BOTTLE (67877-842-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/be69d9f9-f4ad-4cfe-bab2-e07186b25c1e

  • NADAC price for package 67877084201

    GET /v1/drugs/nadac/67877084201

  • NADAC price for package 67877084205

    GET /v1/drugs/nadac/67877084205

  • NADAC price for package 67877084210

    GET /v1/drugs/nadac/67877084210

Use it

Look up 67877-842 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67877-842 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67877-842. 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.