NDC product
Dexmedetomidine Hydrochloride
NDC 36000-262 · Baxter Healthcare Corporation
Key facts
| Product NDC | 36000-262 |
|---|---|
| Proprietary name | Dexmedetomidine Hydrochloride |
| Nonproprietary name | dexmedetomidine hydrochloride |
| Substances | DEXMEDETOMIDINE HYDROCHLORIDE |
| Dosage form | INJECTION, SOLUTION, CONCENTRATE |
| Route | INTRAVENOUS |
| Labeler | Baxter Healthcare Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA208103 |
| Pharmacologic classes | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE] |
| Marketing start | Apr 16, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: