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Glimepiride

NDC 71335-2409, Glimepiride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2409
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202112
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2409 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE4 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
71335-2409-17133524090130 TABLET in 1 BOTTLE (71335-2409-1)
71335-2409-27133524090260 TABLET in 1 BOTTLE (71335-2409-2)
71335-2409-37133524090390 TABLET in 1 BOTTLE (71335-2409-3)
71335-2409-471335240904180 TABLET in 1 BOTTLE (71335-2409-4)
71335-2409-571335240905100 TABLET in 1 BOTTLE (71335-2409-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0b12d4ab-fa0c-44d5-888c-265dbb661561

Use it

Look up 71335-2409 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2409 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2409. 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.