FDA NDC Directory · JSON-LD · Markdown
NDC 51316-210 · HUMAN OTC DRUG · SPRAY
| Labeler / Manufacturer | CVS Pharmacy, Inc |
|---|---|
| Marketing category | Abbreviated NDA (generic) · App ANDA217992 |
| Dosage form / route | SPRAY · NASAL |
| Active ingredients | NALOXONE HYDROCHLORIDE (4 mg/.1mL) |
| Marketing started | 20240424 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).