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Glimepiride

NDC 68001-585, Glimepiride, tablet, from BluePoint Laboratories.

Product NDC
68001-585
Status
Listed
Labeler
BluePoint Laboratories
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091220
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68001-585 \
  -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
68001-585-0068001058500100 TABLET in 1 BOTTLE (68001-585-00)
68001-585-0368001058503500 TABLET in 1 BOTTLE (68001-585-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a01b0466-13f5-4c47-ae55-c5f1527d9414

  • NADAC price for package 68001058500

    GET /v1/drugs/nadac/68001058500

  • NADAC price for package 68001058503

    GET /v1/drugs/nadac/68001058503

Use it

Look up 68001-585 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68001-585 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68001-585. 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.