| NDC Code: |
55154-5384 |
| Proprietary Name: |
Valacyclovir Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
valacyclovir hydrochloride |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
25-09-2012 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078518 |
| Labeler: |
CARDINAL HEALTH |
| Substance Name: |
VALACYCLOVIR HYDROCHLORIDE |
| Active Numerator Strength: |
500 |
| Active Ingredient Unit: |
mg/1 |
| Pharm 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] |
| DEA Schedule: |
|
