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Glimepiride

NDC 55111-321, Glimepiride, tablet, from Dr. Reddy's Laboratories Limited.

Product NDC
55111-321
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/55111-321 \
  -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
55111-321-0155111032101100 TABLET in 1 BOTTLE (55111-321-01)
55111-321-0555111032105500 TABLET in 1 BOTTLE (55111-321-05)
55111-321-305511103213030 TABLET in 1 BOTTLE (55111-321-30)
55111-321-7855111032178100 BLISTER PACK in 1 CARTON (55111-321-78) / 1 TABLET in 1 BLISTER PACK (55111-321-79)

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 55111032101

    GET /v1/drugs/nadac/55111032101

  • NADAC price for package 55111032105

    GET /v1/drugs/nadac/55111032105

Use it

Look up 55111-321 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/55111-321 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 55111-321. 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.