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GLYBURIDE

NDC 71335-0069, GLYBURIDE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-0069
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/71335-0069 \
  -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
71335-0069-17133500690130 TABLET in 1 BOTTLE (71335-0069-1)
71335-0069-27133500690260 TABLET in 1 BOTTLE (71335-0069-2)
71335-0069-37133500690390 TABLET in 1 BOTTLE (71335-0069-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9cdd30e7-512a-4f00-a4de-0a154d143ce9

Use it

Look up 71335-0069 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-0069 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-0069. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.