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Glyburide

NDC 0093-9433, glyburide, tablet, from TEVA Pharmaceuticals USA Inc.

Product NDC
0093-9433
Status
Listed
Labeler
TEVA Pharmaceuticals USA Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA017532
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0093-9433 \
  -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
0093-9433-0100093943301100 TABLET in 1 BOTTLE (0093-9433-01)
0093-9433-0500093943305500 TABLET in 1 BOTTLE (0093-9433-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/50d16f1d-c814-4411-8749-62561321ecce

  • NADAC price for package 00093943301

    GET /v1/drugs/nadac/00093943301

Use it

Look up 0093-9433 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0093-9433 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0093-9433. 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.