Naloxone Hydrochloride
NDC 84549-072, Naloxone Hydrochloride, injection, solution, from ProPharma Distribution.
- Product NDC
- 84549-072
- Status
- Listed
- Labeler
- ProPharma Distribution
- 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/84549-072 \ -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 |
|---|---|---|
| 84549-072-10 | 84549007210 | 10 mL in 1 VIAL, GLASS (84549-072-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/3f2bb95a-aeca-c0b7-e063-6394a90a627b
Use it
Look up 84549-072 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/84549-072 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 84549-072. 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.