| NDC Code | 59762-8398-6 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (59762-8398-6) |
|---|
| Product NDC | 59762-8398 |
|---|
| 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 | 20100524 |
|---|
| End Marketing Date | 20141231 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090682 |
|---|
| Manufacturer | Greenstone LLC |
|---|
| 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 [Chemical/Ingredient] |
|---|