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Glimepiride

NDC 42571-102, Glimepiride, tablet, from Micro Labs Limited.

Product NDC
42571-102
Status
Listed
Labeler
Micro Labs Limited
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/42571-102 \
  -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
42571-102-0142571010201100 TABLET in 1 BOTTLE (42571-102-01)
42571-102-0542571010205500 TABLET in 1 BOTTLE (42571-102-05)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/60e9397e-83b9-489e-9683-6f87e458bbaa

Use it

Look up 42571-102 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42571-102 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42571-102. 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.