| NDC Code | 42291-972-01 |
|---|
| Package Description | 100 mL in 1 BOTTLE (42291-972-01) |
|---|
| Product NDC | 42291-972 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valganciclovir Hydrochloride For Oral |
|---|
| Non-Proprietary Name | Valganciclovir Hydrochloride |
|---|
| Dosage Form | POWDER, FOR SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20231017 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205220 |
|---|
| Manufacturer | AvKARE |
|---|
| Substance Name | VALGANCICLOVIR HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], DNA Polymerase Inhibitors [MoA], Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT] |
|---|