NDC product
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE
NDC 0781-3495 · Sandoz Inc.
Key facts
| Product NDC | 0781-3495 |
|---|---|
| Proprietary name | DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE |
| Nonproprietary name | DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE |
| Substances | DEXMEDETOMIDINE HYDROCHLORIDE |
| Dosage form | INJECTION |
| Route | INTRAVENOUS |
| Labeler | Sandoz Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA209065 |
| Pharmacologic classes | Adrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC], General Anesthesia [PE] |
| Marketing start | Jun 12, 2020 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
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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: