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Glimepiride

NDC 71921-215, Glimepiride, tablet, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-215
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202112
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-215 \
  -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
71921-215-0171921021501100 TABLET in 1 BOTTLE (71921-215-01)
71921-215-5071921021550500 TABLET in 1 BOTTLE (71921-215-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8ff0de99-272e-4e68-9caf-69f3f146ac29

  • NADAC price for package 71921021501

    GET /v1/drugs/nadac/71921021501

  • NADAC price for package 71921021550

    GET /v1/drugs/nadac/71921021550

Use it

Look up 71921-215 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-215 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-215. 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.