Fludarabine phosphate
Active substance: fludarabine
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · FLUDARABINE PHOSPHATE 50 mg/2mL
United StatesActive
Marketing holder: Actavis Pharma, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- FLUDARABINE PHOSPHATE · 50 mg/2mL
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208e-a3f6-7d06-8417-9c2dc6b7e042,01a12091-75e4-7476-b930-32e2606bc431,01a12095-d657-76e1-9709-8a0f0f68e6e6,01a1209a-e4cd-7f08-af20-5549f5f4c1b8,01a1209b-5dd0-78e3-92a1-a5c26368e031;count=6 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 45963-609
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAVENOUS
Sources
- product · openFDA NDC · 45963-609 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 45963-609 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 45963-609 · Verified 2026-10-09 · open in source