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Glimepiride

NDC 55111-322, Glimepiride, tablet, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-322
Status
Listed
Labeler
Dr. Reddy's Laboratories Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA077091
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/55111-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE4 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
55111-322-0155111032201100 TABLET in 1 BOTTLE (55111-322-01)
55111-322-0555111032205500 TABLET in 1 BOTTLE (55111-322-05)
55111-322-305511103223030 TABLET in 1 BOTTLE (55111-322-30)
55111-322-7855111032278100 BLISTER PACK in 1 CARTON (55111-322-78) / 1 TABLET in 1 BLISTER PACK (55111-322-79)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/07ad4366-4b21-f633-49f3-c2b35f88168d

  • NADAC price for package 55111032201

    GET /v1/drugs/nadac/55111032201

  • NADAC price for package 55111032205

    GET /v1/drugs/nadac/55111032205

Use it

Look up 55111-322 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-322 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-322. 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.