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Glimepiride

NDC 71205-779, Glimepiride, tablet, from Proficient Rx LP.

Product NDC
71205-779
Status
Listed
Labeler
Proficient Rx LP
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/71205-779 \
  -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
71205-779-307120507793030 TABLET in 1 BOTTLE (71205-779-30)
71205-779-607120507796060 TABLET in 1 BOTTLE (71205-779-60)
71205-779-7871205077978180 TABLET in 1 BOTTLE (71205-779-78)
71205-779-907120507799090 TABLET in 1 BOTTLE (71205-779-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e12ab052-e3d6-4246-b727-f1e3f9057f09

Use it

Look up 71205-779 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-779 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-779. 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.