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GLYBURIDE

NDC 71335-0150, GLYBURIDE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0150
Status
Listed
Labeler
Bryant Ranch Prepack
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/71335-0150 \
  -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
71335-0150-17133501500130 TABLET in 1 BOTTLE (71335-0150-1)
71335-0150-271335015002120 TABLET in 1 BOTTLE (71335-0150-2)
71335-0150-371335015003100 TABLET in 1 BOTTLE (71335-0150-3)
71335-0150-47133501500460 TABLET in 1 BOTTLE (71335-0150-4)
71335-0150-57133501500590 TABLET in 1 BOTTLE (71335-0150-5)
71335-0150-671335015006180 TABLET in 1 BOTTLE (71335-0150-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/05341afe-5b7a-462a-a196-689cb09f83fc

Use it

Look up 71335-0150 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0150 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0150. 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.