FDA NDC Directory · JSON-LD · Markdown
NDC 0404-9922 · HUMAN PRESCRIPTION DRUG · INJECTION
| Generic name | naloxone hydrochloride |
|---|---|
| Labeler / Manufacturer | Henry Schein, Inc |
| Marketing category | Abbreviated NDA (generic) · App ANDA072076 |
| Dosage form / route | INJECTION · PARENTERAL |
| Active ingredients | NALOXONE HYDROCHLORIDE (1 mg/mL) |
| Marketing started | 20220113 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).