Xyntha
NDC 58394-013, antihemophilic factor (recombinant), kit, from Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC.
- Product NDC
- 58394-013
- Status
- Listed
- Labeler
- Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
- Dosage form
- KIT
- Route
- —
- Product type
- PLASMA DERIVATIVE
- Marketing category
- BLA
- Application
- BLA125264
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/58394-013 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 58394-013-01 | 58394001301 | 1 KIT in 1 CARTON (58394-013-01) * 4 mL in 1 SYRINGE (58394-018-01) * 1 mL in 1 PACKET * 4 mL in 1 VIAL, SINGLE-USE (58394-113-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=58394-013
Use it
Look up 58394-013 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/58394-013 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 58394-013. 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.