70436-030Level 3
acyclovir (acyclovir)
**Product type:** Human Prescription Drug
**Active ingredient:** ACYCLOVIR SODIUM
**Strength:** 50 mg/mL
**Dosage form:** Injection, Solution
**Route:** Intravenous
**Labeler:** Slate Run Pharmaceuticals, LLC
**Marketing category:** ANDA (ANDA218111)
**Pharmacologic class:** DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
GET
/api/v1/systems/ndc_fda/nodes/70436-030Hierarchy Explorer
Loading...
Cross-system equivalences0
No cross-system equivalences mapped for this node.