Ganciclovir Sodium 70436-0231
Product NDC
70436-0231- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA204204
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ganciclovir Sodium | 500 mg/10mL |
Drug Class
Cytomegalovirus Nucleoside Analog DNA Polymerase Inhibitor [EPC]DNA Polymerase Inhibitors [MoA]Nucleoside Analog Antiviral [EPC]
Packaging Options(1)
25 VIAL in 1 CARTON (70436-231-55) / 10 mL in 1 VIAL