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Glimepiride

NDC 68788-8432, Glimepiride, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8432
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202759
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8432 \
  -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
68788-8432-36878884320330 TABLET in 1 BOTTLE (68788-8432-3)
68788-8432-66878884320660 TABLET in 1 BOTTLE (68788-8432-6)
68788-8432-96878884320990 TABLET in 1 BOTTLE (68788-8432-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/744a5cca-7863-491a-b43a-1b649791702c

Use it

Look up 68788-8432 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8432 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8432. 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.