| NDC Code | 63739-077-10 |
|---|
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-077-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
|---|
| Product NDC | 63739-077 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Valacyclovir |
|---|
| Non-Proprietary Name | Valacyclovir |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20220317 |
|---|
| End Marketing Date | 20260131 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA203047 |
|---|
| Manufacturer | McKesson Corporation dba SKY Packaging |
|---|
| 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] |
|---|