Acyclovir 70436-0030-82

Package NDC

70436-0030-82

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]

Selected Package

70436-0030-82Selected

10 VIAL, SINGLE-DOSE in 1 CARTON (70436-030-82) / 10 mL in 1 VIAL, SINGLE-DOSE