Naloxone Hydrochloride
NDC 72572-450, Nalxone Hydrochloride, injection, from Civica, Inc..
- Product NDC
- 72572-450
- Status
- Listed
- Labeler
- Civica, Inc.
- Dosage form
- INJECTION
- Route
- INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA070299
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72572-450 \ -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 |
|---|---|---|
| 72572-450-25 | 72572045025 | 25 VIAL in 1 CARTON (72572-450-25) / 1 mL in 1 VIAL (72572-450-01) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/21d20dff-6efe-481e-a5a0-9c80ded73ca9Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=72572-450
Use it
Look up 72572-450 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72572-450 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72572-450. 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.