Valacyclovir Hydrochloride 72789-0263
Product NDC
72789-0263- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- 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(5)
6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-06)
10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-10)
14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14)
28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-28)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-90)