Composition
- Active ingredients
- ACYCLOVIR SODIUM EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ACYCLOVIR SODIUM EQ 250MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA018603-003 · Discontinued
- ACYCLOVIR SODIUM EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableThis page
- ACYCLOVIR SODIUM EQ 1GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA018603-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA018603.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Zovirax
- Active substance
- acyclovir sodium
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Glaxosmithkline
- Status
- Discontinued
- FDA approval
- 22 Oct 1982
- Application
- NDA018603-001