NDC Code | 50090-2101-2 |
Package Description | 30 TABLET in 1 BOTTLE (50090-2101-2) |
Product NDC | 50090-2101 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Valacyclovir Hydrochloride |
Non-Proprietary Name | Valacyclovir Hydrochloride |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20100524 |
Marketing Category Name | ANDA |
Application Number | ANDA077135 |
Manufacturer | A-S Medication Solutions |
Substance Name | VALACYCLOVIR HYDROCHLORIDE |
Strength | 1000 |
Strength Unit | mg/1 |
Pharmacy Classes | DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT] |