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Famotidine

NDC 63629-7013, Famotidine, tablet, from Bryant Ranch Prepack.

Product NDC
63629-7013
Status
Listed
Labeler
Bryant Ranch Prepack
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/63629-7013 \
  -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
63629-7013-16362970130130 TABLET in 1 BOTTLE (63629-7013-1)
63629-7013-26362970130260 TABLET in 1 BOTTLE (63629-7013-2)
63629-7013-36362970130390 TABLET in 1 BOTTLE (63629-7013-3)
63629-7013-46362970130410 TABLET in 1 BOTTLE (63629-7013-4)
63629-7013-56362970130520 TABLET in 1 BOTTLE (63629-7013-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/81f24752-3474-3013-0013-5570c8e7baf7

Use it

Look up 63629-7013 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-7013 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-7013. 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.