NDC Code | 59746-324-90 |
Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59746-324-90) |
Product NDC | 59746-324 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Valacyclovir Hydrochloride |
Non-Proprietary Name | Valacyclovir Hydrochloride |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20120405 |
Marketing Category Name | ANDA |
Application Number | ANDA201506 |
Manufacturer | Jubilant Cadista Pharmaceuticals Inc. |
Substance Name | VALACYCLOVIR HYDROCHLORIDE |
Strength | 500 |
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] |