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Glimepiride

NDC 68788-4191, Glimepiride, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-4191
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/68788-4191 \
  -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
68788-4191-36878841910330 TABLET in 1 BOTTLE (68788-4191-3)
68788-4191-66878841910660 TABLET in 1 BOTTLE (68788-4191-6)
68788-4191-96878841910990 TABLET in 1 BOTTLE (68788-4191-9)

Linked data

RxNorm, label and prices

RxNorm concepts

RxNorm links no concept to this product's packages.

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/aa533cde-4b32-450e-b080-127351524678

Use it

Look up 68788-4191 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-4191 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-4191. 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.