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Cytovene
Cytovene - 0004-6940-03 - (ganciclovir sodium)
Drug Information of Cytovene
| Product NDC: | 0004-6940 |
| Proprietary Name: | Cytovene |
| Non Proprietary Name: | ganciclovir sodium |
| Active Ingredient(s): | 500 mg/10mL & nbsp; ganciclovir sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cytovene
| Product NDC: | 0004-6940 |
| Labeler Name: | Genentech, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA019661 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19890623 |
Package Information of Cytovene
| Package NDC: | 0004-6940-03 |
| Package Description: | 25 VIAL in 1 CARTON (0004-6940-03) > 10 mL in 1 VIAL |
NDC Information of Cytovene
| NDC Code | 0004-6940-03 |
| Proprietary Name | Cytovene |
| Package Description | 25 VIAL in 1 CARTON (0004-6940-03) > 10 mL in 1 VIAL |
| Product NDC | 0004-6940 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ganciclovir sodium |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19890623 |
| Marketing Category Name | NDA |
| Labeler Name | Genentech, Inc. |
| Substance Name | GANCICLOVIR SODIUM |
| Strength Number | 500 |
| Strength Unit | mg/10mL |
| Pharmaceutical Classes | Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA],Nucleoside Analog [Chemical/Ingredient],Nucleoside Analog Antiviral [EPC] |
