REXTOVY
NDC 76329-3669, Naloxone Hydrochloride, spray, from International Medication Systems, Ltd..
- Product NDC
- 76329-3669
- Status
- Listed
- Labeler
- International Medication Systems, Ltd.
- Dosage form
- SPRAY
- Route
- NASAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208969
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/76329-3669 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NALOXONE HYDROCHLORIDE4 mg/.25mL
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 76329-3669-2 | 76329366902 | 2 CONTAINER in 1 CONTAINER (76329-3669-2) / .25 mL in 1 CONTAINER |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/fe9735db-c57e-44a8-bffb-b87a84c2a6f3
Use it
Look up 76329-3669 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/76329-3669 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 76329-3669. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.