Glimepiride
NDC 43063-630, Glimepiride, tablet, from PD-Rx Pharmaceuticals, Inc..
- Product NDC
- 43063-630
- 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/43063-630 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- GLIMEPIRIDE2 mg/1
Pharmacologic classes
Sulfonylurea Compounds [CS]; Sulfonylurea [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 43063-630-30 | 43063063030 | 30 TABLET in 1 BOTTLE, PLASTIC (43063-630-30) |
| 43063-630-90 | 43063063090 | 90 TABLET in 1 BOTTLE, PLASTIC (43063-630-90) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/1b3c7d74-f80b-4fb1-8dca-66880af5d3fc
Use it
Look up 43063-630 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43063-630 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43063-630. 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.