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GLYBURIDE

NDC 51655-492, GLYBURIDE, tablet, from Northwind Health Company, LLC.

Product NDC
51655-492
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090937
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLYBURIDE5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
51655-492-255165504922560 TABLET in 1 BOTTLE, PLASTIC (51655-492-25)
51655-492-265165504922690 TABLET in 1 BOTTLE, PLASTIC (51655-492-26)
51655-492-525165504925230 TABLET in 1 BOTTLE, PLASTIC (51655-492-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d9cb9251-7b31-72a0-e053-2a95a90a4315

Use it

Look up 51655-492 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-492 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-492. 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.