CUPRIC CHLORIDE
NDC 51754-0103, cupric chloride, injection, solution, from Exela Pharma Sciences, LLC.
- Product NDC
- 51754-0103
- Status
- Listed
- Labeler
- Exela Pharma Sciences, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA212071
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/51754-0103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CUPRIC CHLORIDE.4 mg/mL
| Package NDC | NDC-11 | Package |
|---|---|---|
| 51754-0103-3 | 51754010303 | 10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSE |
| 51754-0103-4 | 51754010304 | 25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/daaa6f3a-148e-4f1c-bd44-bb2242145b88
Use it
Look up 51754-0103 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/51754-0103 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 51754-0103. 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.