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Glimepiride

NDC 71335-2561, Glimepiride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2561
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/71335-2561 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE1 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
71335-2561-17133525610130 TABLET in 1 BOTTLE (71335-2561-1)
71335-2561-27133525610260 TABLET in 1 BOTTLE (71335-2561-2)
71335-2561-37133525610390 TABLET in 1 BOTTLE (71335-2561-3)
71335-2561-471335256104100 TABLET in 1 BOTTLE (71335-2561-4)
71335-2561-57133525610520 TABLET in 1 BOTTLE (71335-2561-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/661b5b13-6334-4965-8dc5-709e19080584

Use it

Look up 71335-2561 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2561 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2561. 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.