| NDC Code | 63304-905-03 |
|---|
| Package Description | 10 TABLET, FILM COATED in 1 BOTTLE (63304-905-03) |
|---|
| Product NDC | 63304-905 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valacyclovir |
|---|
| Non-Proprietary Name | Valacyclovir |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20201219 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076588 |
|---|
| Manufacturer | SUN PHARMACEUTICAL INDUSTRIES, INC. |
|---|
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
|---|
| Strength | 1 |
|---|
| Strength Unit | g/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] |
|---|