Home
>
National Drug Code (NDC)
>
Valcyte
Valcyte - 0004-0039-09 - (valganciclovir hydrochloride)
Drug Information of Valcyte
| Product NDC: | 0004-0039 |
| Proprietary Name: | Valcyte |
| Non Proprietary Name: | valganciclovir hydrochloride |
| Active Ingredient(s): | 50 mg/mL & nbsp; valganciclovir hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Valcyte
| Product NDC: | 0004-0039 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022257 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090828 |
Package Information of Valcyte
| Package NDC: | 0004-0039-09 |
| Package Description: | 1 BOTTLE, GLASS in 1 CARTON (0004-0039-09) > 100 mL in 1 BOTTLE, GLASS |
NDC Information of Valcyte
| NDC Code | 0004-0039-09 |
| Proprietary Name | Valcyte |
| Package Description | 1 BOTTLE, GLASS in 1 CARTON (0004-0039-09) > 100 mL in 1 BOTTLE, GLASS |
| Product NDC | 0004-0039 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | valganciclovir hydrochloride |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 20090828 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | VALGANCICLOVIR HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
