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GLYBURIDE

NDC 23155-057, GLYBURIDE, tablet, from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..

Product NDC
23155-057
Status
Listed
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
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/23155-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLYBURIDE2.5 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
23155-057-0123155005701100 TABLET in 1 BOTTLE (23155-057-01)
23155-057-10231550057101000 TABLET in 1 BOTTLE (23155-057-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/33418bba-c5ea-4c0f-9d28-31dc2724c6c3

  • NADAC price for package 23155005701

    GET /v1/drugs/nadac/23155005701

Use it

Look up 23155-057 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/23155-057 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 23155-057. 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.