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Probenecid

NDC 72162-2237, Probenecid, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-2237
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA080966
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2237 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PROBENECID500 mg/1
Package NDCNDC-11Package
72162-2237-172162223701100 TABLET, FILM COATED in 1 BOTTLE (72162-2237-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6aec72b5-a9f4-45a3-82a6-7d3de64ba5e5

Use it

Look up 72162-2237 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2237 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2237. 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.