Zinc Sulfate
NDC 65219-403, Zinc Sulfate, injection, solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 65219-403
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216145
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65219-403 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ZINC SULFATE3 mg/mL
Pharmacologic classes
Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65219-403-03 | 65219040303 | 25 VIAL in 1 TRAY (65219-403-03) / 10 mL in 1 VIAL (65219-403-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/37d54dcd-b720-4168-bfb2-c8f381466aac
Use it
Look up 65219-403 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65219-403 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65219-403. 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.