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Glimepiride

NDC 65862-580, Glimepiride, tablet, from Aurobindo Pharma Limited.

Product NDC
65862-580
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/65862-580 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE2 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
65862-580-0165862058001100 TABLET in 1 BOTTLE (65862-580-01)
65862-580-0565862058005500 TABLET in 1 BOTTLE (65862-580-05)
65862-580-99658620580991000 TABLET in 1 BOTTLE (65862-580-99)

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 65862-580 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-580 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-580. 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.