Acyclovir - ACYCLOVIR SODIUM
Navigation: NDC > Supplier starting with: A > APP PHARMACEUTICALS, LLC| Field | Value |
|---|---|
| NDC Code: | 63323-105 |
| Proprietary Name: | Acyclovir |
| Suffix: | |
| Non-Proprietary Name: | ACYCLOVIR SODIUM |
| Dosage Form: | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Method: | INTRAVENOUS |
| Original Marketing Date: | 17-10-2000 |
| Category Name: | ANDA |
| Application Number: | ANDA075015 |
| Labeler: | APP PHARMACEUTICALS, LLC |
| Substance Name: | ACYCLOVIR SODIUM |
| Active Numerator Strength: | 50 |
| Active Ingredient Unit: | mg/mL |
| 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: |