Valacyclovir Hydrochloride 00904-6565
Product NDC
00904-6565- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 24, 2010
- Listing Expires
- December 31, 2027
- Application
- ANDA090682
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Valacyclovir Hydrochloride | 500 mg/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(2)
30 BLISTER PACK in 1 CARTON (0904-6565-07) / 1 TABLET, FILM COATED in 1 BLISTER PACK
100 BLISTER PACK in 1 CARTON (0904-6565-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK