United States · FDA National Drug Code directory
Xyntha
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 58394-023_9b1ef7a8-35e5-4b97-9907-fc807d47e0fc
- Product NDC
- 58394-023
- Form
- KIT
- Composition / generic term
- antihemophilic factor (recombinant)
- Labeler
- Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 20111201
- Source listing expiry
- 20271231
Source-listed ingredients
Separate ingredient quantities are not available in this snapshot. Any composition term above is preserved as source text.
These values do not establish equivalence or a dose recommendation.
Packages
- 1 KIT in 1 CARTON (58394-023-03) * 4 mL in 1 SYRINGE (58394-123-03) * 1 mL in 1 PACKET · 58394-023-03
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →