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Glimepiride

NDC 71335-9655, Glimepiride, tablet, from Bryant Ranch Prepack.

Product NDC
71335-9655
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202759
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9655 \
  -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
71335-9655-17133596550130 TABLET in 1 BOTTLE (71335-9655-1)
71335-9655-27133596550260 TABLET in 1 BOTTLE (71335-9655-2)
71335-9655-37133596550390 TABLET in 1 BOTTLE (71335-9655-3)
71335-9655-471335965504100 TABLET in 1 BOTTLE (71335-9655-4)
71335-9655-57133596550520 TABLET in 1 BOTTLE (71335-9655-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/248c3cb3-4501-4b85-bd1d-0624b6afda2c

Use it

Look up 71335-9655 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-9655 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-9655. 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.