NALOXONE HYDROCHLORIDE
NDC 50090-6963, naloxone hydrochloride, spray, from A-S Medication Solutions.
- Product NDC
- 50090-6963
- Status
- Listed
- Labeler
- A-S Medication Solutions
- Dosage form
- SPRAY
- Route
- NASAL
- Product type
- HUMAN OTC DRUG
- Marketing category
- ANDA
- Application
- ANDA211951
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6963 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- NALOXONE HYDROCHLORIDE4 mg/.1mL
Pharmacologic classes
Opioid Antagonist [EPC]; Opioid Antagonists [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 50090-6963-0 | 50090696300 | 2 VIAL, SINGLE-DOSE in 1 CARTON (50090-6963-0) / .1 mL in 1 VIAL, SINGLE-DOSE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.
Use it
Look up 50090-6963 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50090-6963 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50090-6963. 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.