| NDC Code | 65862-753-05 |
|---|
| Package Description | 500 TABLET in 1 BOTTLE (65862-753-05) |
|---|
| Product NDC | 65862-753 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valganciclovir Hydrochloride |
|---|
| Non-Proprietary Name | Valganciclovir Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204750 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | VALGANCICLOVIR HYDROCHLORIDE |
|---|
| Strength | 450 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], DNA Polymerase Inhibitors [MoA], Nucleoside Analog Antiviral [EPC], Nucleoside Analog [EXT] |
|---|