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Glimepiride

NDC 65862-581, Glimepiride, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-581
Status
Listed
Labeler
Aurobindo Pharma Limited
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/65862-581 \
  -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
65862-581-0165862058101100 TABLET in 1 BOTTLE (65862-581-01)
65862-581-0565862058105500 TABLET in 1 BOTTLE (65862-581-05)
65862-581-2565862058125250 TABLET in 1 BOTTLE (65862-581-25)
65862-581-99658620581991000 TABLET in 1 BOTTLE (65862-581-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/28eefc95-d92e-4555-b6c5-2933860b0610

Use it

Look up 65862-581 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-581 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-581. 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.