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Famotidine

NDC 43063-696, Famotidine, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-696
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/43063-696 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43063-696-304306306963030 TABLET in 1 BOTTLE, PLASTIC (43063-696-30)
43063-696-904306306969090 TABLET in 1 BOTTLE, PLASTIC (43063-696-90)
43063-696-9343063069693180 TABLET in 1 BOTTLE, PLASTIC (43063-696-93)
43063-696-95430630696951000 TABLET in 1 BOTTLE, PLASTIC (43063-696-95)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/09ef39a4-c6b3-4395-8211-3f551dc44830

Use it

Look up 43063-696 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-696 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-696. 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.