Ganciclovir
- Strength
- 500 mg/10mL
- Form
- Injection, Powder, Lyophilized, For Solution
- Class
- Cytomegalovirus Nucleoside Analog DNA P…
Endo USA, Inc.
ganciclovir sodium
Listed by Slate Run Pharmaceuticals, LLC
| Dosage form | Injection, Powder, Lyophilized, For Solution |
|---|---|
| Route | Intravenous |
| Drug class | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor; Nucleoside Analog Antiviral |
| Approval route | ANDA — approved generic |
| NDC code | 70436-089 |
| FDA application | ANDA204204 |
| RxNorm concept | 310442 |
| Package sizes listed | 1 |
| Marketed since | January 2019 |
Same active ingredient, different manufacturer, strength or form. Products matching on both ingredient and strength are usually interchangeable — but confirm before switching, especially with modified-release forms.
Endo USA, Inc.
GANCICLOVIR SODIUM
Fresenius Kabi USA, LLC
ganciclovir sodium
Pharmascience Inc.
ganciclovir sodium
Sagent Pharmaceuticals
Ganciclovir sodium
Hikma Pharmaceuticals USA Inc.
Slate Run Pharmaceuticals, LLC
ganciclovir
Bausch & Lomb Incorporated
Information only, not medical advice. Nothing on this page indicates that a medication is safe or suitable for you. Speak to a prescriber or pharmacist before starting, stopping or switching any medicine.
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