NDC product
naloxone hydrochloride
NDC 36000-308 · Baxter Healthcare Corporation
Key facts
| Product NDC | 36000-308 |
|---|---|
| Proprietary name | naloxone hydrochloride |
| Nonproprietary name | naloxone hydrochloride |
| Substances | NALOXONE HYDROCHLORIDE |
| Dosage form | INJECTION, SOLUTION |
| Route | INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS |
| Labeler | Baxter Healthcare Corporation |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA214785 |
| Pharmacologic classes | Opioid Antagonist [EPC], Opioid Antagonists [MoA] |
| Marketing start | Jan 29, 2021 |
| 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: