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glyburide

NDC 68382-658, glyburide, tablet, from Zydus Pharmaceuticals (USA) Inc..

Product NDC
68382-658
Status
Listed
Labeler
Zydus Pharmaceuticals (USA) Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206749
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68382-658 \
  -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
68382-658-0168382065801100 TABLET in 1 BOTTLE (68382-658-01)
68382-658-0568382065805500 TABLET in 1 BOTTLE (68382-658-05)
68382-658-066838206580630 TABLET in 1 BOTTLE (68382-658-06)
68382-658-10683820658101000 TABLET in 1 BOTTLE (68382-658-10)
68382-658-166838206581690 TABLET in 1 BOTTLE (68382-658-16)
68382-658-776838206587710 BLISTER PACK in 1 CARTON (68382-658-77) / 10 TABLET in 1 BLISTER PACK (68382-658-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/87781ea8-62ec-483c-a4dd-8c965ce59485

Use it

Look up 68382-658 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68382-658 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68382-658. 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.