Dexmedetomidine Hydrochloride
NDC 25021-617, Dexmedetomidine Hydrochloride, injection, from Sagent Pharmaceuticals.
- Product NDC
- 25021-617
- Status
- Listed
- Labeler
- Sagent Pharmaceuticals
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209307
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/25021-617 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DEXMEDETOMIDINE HYDROCHLORIDE4 ug/mL
Pharmacologic classes
Adrenergic alpha2-Agonists [MoA]; Central alpha-2 Adrenergic Agonist [EPC]; General Anesthesia [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 25021-617-82 | 25021061782 | 20 BAG in 1 CARTON (25021-617-82) / 100 mL in 1 BAG |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/65885aef-faaf-4dec-a180-9a657f738bbc
Use it
Look up 25021-617 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/25021-617 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 25021-617. 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.