NDC Code | 43598-356-30 |
Package Description | 30 TABLET in 1 BOTTLE (43598-356-30) |
Product NDC | 43598-356 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Valganciclovir Hydrochloride |
Non-Proprietary Name | Valganciclovir Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20171212 |
Marketing Category Name | ANDA |
Application Number | ANDA206876 |
Manufacturer | Dr. Reddy's Laboratories Inc |
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] |