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Glimepiride

NDC 61442-117, Glimepiride, tablet, from Carlsbad Technology, Inc..

Product NDC
61442-117
Status
Listed
Labeler
Carlsbad Technology, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077911
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/61442-117 \
  -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
61442-117-0161442011701100 TABLET in 1 BOTTLE (61442-117-01)
61442-117-0561442011705500 TABLET in 1 BOTTLE (61442-117-05)
61442-117-10614420117101000 TABLET in 1 BOTTLE (61442-117-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/72d88c6d-2f0a-4bf8-aa7f-1e1811794187

  • NADAC price for package 61442011701

    GET /v1/drugs/nadac/61442011701

  • NADAC price for package 61442011705

    GET /v1/drugs/nadac/61442011705

Use it

Look up 61442-117 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/61442-117 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 61442-117. 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.