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Glimepiride

NDC 43063-121, Glimepiride, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
43063-121
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
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/43063-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • GLIMEPIRIDE1 mg/1

Pharmacologic classes

Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]

Package NDCNDC-11Package
43063-121-304306301213030 TABLET in 1 BOTTLE, PLASTIC (43063-121-30)
43063-121-904306301219090 TABLET in 1 BOTTLE, PLASTIC (43063-121-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/657f1b51-2f82-44f6-a23d-97f4b34b3c45

Use it

Look up 43063-121 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43063-121 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43063-121. 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.