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Famotidine

NDC 60687-595, Famotidine, tablet, film coated, from American Health Packaging.

Product NDC
60687-595
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206530
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-595 \
  -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
60687-595-0160687059501100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-595-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-595-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3a583080-6771-4246-a221-2491e9e5d8af

  • NADAC price for package 60687059501

    GET /v1/drugs/nadac/60687059501

Use it

Look up 60687-595 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-595 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-595. 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.