| NDC Code | 21695-832-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (21695-832-30) |
|---|
| Product NDC | 21695-832 |
|---|
| 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 | 20091203 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077135 |
|---|
| Manufacturer | Rebel Distributors Corp |
|---|
| Substance Name | VALACYCLOVIR HYDROCHLORIDE |
|---|
| Strength | 500 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],DNA Polymerase Inhibitors [MoA] |
|---|