Acyclovir
Active substance: acyclovir
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · ACYCLOVIR SODIUM 500 mg/1
United StatesActive
Marketing holder: Hikma Pharmaceuticals USA Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
Composition
- ACYCLOVIR SODIUM · 500 mg/1
Registration
- Registration number
- 0143-9657
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- INTRAVENOUS
Sources
- product · openFDA NDC · 0143-9657 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0143-9657 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0143-9657 · Verified 2026-10-09 · open in source