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Glimepiride

NDC 68788-8728, Glimepiride, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8728
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-8728 \
  -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
68788-8728-168788872801100 TABLET in 1 BOTTLE (68788-8728-1)
68788-8728-36878887280330 TABLET in 1 BOTTLE (68788-8728-3)
68788-8728-66878887280660 TABLET in 1 BOTTLE (68788-8728-6)
68788-8728-96878887280990 TABLET in 1 BOTTLE (68788-8728-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f69e36b9-4940-4f01-b5ea-59dc66dc1e87

Use it

Look up 68788-8728 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8728 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8728. 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.