| NDC Code | 0143-9299-10 |
|---|
| Package Description | 10 VIAL in 1 BOX (0143-9299-10) / 10 mL in 1 VIAL (0143-9299-01) |
|---|
| Product NDC | 0143-9299 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Ganciclovir |
|---|
| Non-Proprietary Name | Ganciclovir Sodium |
|---|
| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
|---|
| Usage | INTRAVENOUS |
|---|
| Start Marketing Date | 20210617 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076222 |
|---|
| Manufacturer | Hikma Pharmaceuticals USA Inc. |
|---|
| Substance Name | GANCICLOVIR SODIUM |
|---|
| 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] |
|---|