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Glimepiride

NDC 16571-774, Glimepiride, tablet, from Rising Pharma Holdings, Inc..

Product NDC
16571-774
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
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/16571-774 \
  -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
16571-774-0116571077401100 TABLET in 1 BOTTLE (16571-774-01)
16571-774-5016571077450500 TABLET in 1 BOTTLE (16571-774-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/48ada723-8144-497d-afd6-a8c52a1dd3ff

  • NADAC price for package 16571077401

    GET /v1/drugs/nadac/16571077401

  • NADAC price for package 16571077450

    GET /v1/drugs/nadac/16571077450

Use it

Look up 16571-774 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16571-774 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16571-774. 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.