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Famotidine

NDC 71610-399, Famotidine, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-399
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078916
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-399 \
  -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
71610-399-307161003993030 TABLET in 1 BOTTLE (71610-399-30)
71610-399-607161003996090 TABLET in 1 BOTTLE (71610-399-60)
71610-399-8071610039980180 TABLET in 1 BOTTLE (71610-399-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b1839d23-20f4-4651-a7d2-8bc3a7583917

Use it

Look up 71610-399 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-399 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-399. 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.