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Famotidine

NDC 64980-737, Famotidine, powder, for suspension, from RISING PHARMA HOLDINGS, INC..

Product NDC
64980-737
Status
Listed
Labeler
RISING PHARMA HOLDINGS, INC.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217655
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64980-737 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FAMOTIDINE40 mg/5mL

Pharmacologic classes

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

Package NDCNDC-11Package
64980-737-506498007375050 mL in 1 BOTTLE (64980-737-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c013654e-9cad-4c59-8fea-b00ae1567c18

Use it

Look up 64980-737 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64980-737 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64980-737. 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.