NALOXONE HYDROCHLORIDE
NDC 51662-1426, NALOXONE HYDROCHLORIDE, injection, solution, from HF Acquisition Co LLC, DBA HealthFirst.
- Product NDC
- 51662-1426
- Status
- Listed
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207634
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1426 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NALOXONE HYDROCHLORIDE.4 mg/mL
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51662-1426-1 | 51662142601 | 1 VIAL, GLASS in 1 CARTON (51662-1426-1) / 10 mL in 1 VIAL, GLASS |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/9bcff682-1196-7cef-e053-2a95a90aa954
Use it
Look up 51662-1426 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1426 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51662-1426. 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.