Valacyclovir Hydrochloride 51655-0703
Product NDC
51655-0703- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA090682
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Valacyclovir Hydrochloride | 1 g/1 |
Drug Class
DNA Polymerase Inhibitors [MoA]Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC]
Packaging Options(3)
4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-04)
21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-21)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-53)