| NDC Code | 72205-019-01 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (72205-019-01) > 100 mL in 1 BOTTLE |
|---|
| Product NDC | 72205-019 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valganciclovir Hydrochloride |
|---|
| Non-Proprietary Name | Valganciclovir Hydrochloride |
|---|
| Dosage Form | FOR SOLUTION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220217 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA210169 |
|---|
| Manufacturer | Novadoz Pharmaceuticals LLC |
|---|
| 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] |
|---|