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NDC 63187-999, Famotidine, tablet, from Proficient Rx LP.

Product NDC
63187-999
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET
Route
ORAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA075400
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63187-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE10 mg/1

Pharmacologic classes

Histamine H2 Receptor Antagonists [MoA]; Histamine-2 Receptor Antagonist [EPC]

Package NDCNDC-11Package
63187-999-106318709991010 TABLET in 1 BOTTLE (63187-999-10)
63187-999-306318709993030 TABLET in 1 BOTTLE (63187-999-30)
63187-999-606318709996060 TABLET in 1 BOTTLE (63187-999-60)
63187-999-906318709999090 TABLET in 1 BOTTLE (63187-999-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 63187-999 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63187-999 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63187-999. 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.