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Famotidine

NDC 71610-470, Famotidine, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-470
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-470 \
  -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
71610-470-537161004705360 TABLET in 1 BOTTLE, PLASTIC (71610-470-53)
71610-470-607161004706090 TABLET in 1 BOTTLE, PLASTIC (71610-470-60)
71610-470-8071610047080180 TABLET in 1 BOTTLE, PLASTIC (71610-470-80)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/46c6d243-eefc-40ca-8bd4-4c89456f635f

Use it

Look up 71610-470 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-470 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-470. 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.