Glimepiride
NDC 43063-587, Glimepiride, tablet, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 43063-587
- Status
- Listed
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA078181
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43063-587 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLIMEPIRIDE4 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43063-587-30 | 43063058730 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-587-30) |
| 43063-587-90 | 43063058790 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-587-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/58c4261e-e98f-4280-9562-2800956dff14
Use it
Look up 43063-587 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43063-587 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43063-587. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.