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Glimepiride

NDC 82804-065, Glimepiride, tablet, from Proficient Rx LP.

Product NDC
82804-065
Status
Listed
Labeler
Proficient Rx LP
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/82804-065 \
  -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
82804-065-308280400653030 TABLET in 1 BOTTLE (82804-065-30)
82804-065-608280400656060 TABLET in 1 BOTTLE (82804-065-60)
82804-065-7882804006578180 TABLET in 1 BOTTLE (82804-065-78)
82804-065-908280400659090 TABLET in 1 BOTTLE (82804-065-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dbed06f9-7758-4c96-9af0-1ed6103db7df

Use it

Look up 82804-065 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82804-065 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82804-065. 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.