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Glimepiride 3 mg

NDC 72336-641, Glimepiride, tablet, from Lifsa Drugs LLC.

Product NDC
72336-641
Status
Listed
Labeler
Lifsa Drugs LLC
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/72336-641 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE3 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
72336-641-0172336064101100 TABLET in 1 BOTTLE (72336-641-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/51157849-7990-4a8b-ae50-eda1baf93cfa

Use it

Look up 72336-641 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72336-641 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72336-641. 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.