Acyclovir 70436-0030
Product NDC
70436-0030- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218111
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Acyclovir Sodium | 50 mg/mL |
Drug Class
DNA Polymerase Inhibitors [MoA]Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
Packaging Options(1)
10 VIAL, SINGLE-DOSE in 1 CARTON (70436-030-82) / 10 mL in 1 VIAL, SINGLE-DOSE