NDC 0173-0933 – Valtrex
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC0173-0933
Product details
- Brand name
- Valtrex
- Generic name
- valacyclovir hydrochloride
- Labeler
- GlaxoSmithKline LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA · NDA020487
- Marketed since
- August 1, 1995
- Listing expires
- December 31, 2027
- Pharmacologic class
- Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor
Active ingredients
- Valacyclovir Hydrochloride 500 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0173-0933-08 | 30 TABLET, FILM COATED in 1 BOTTLE (0173-0933-08) | Aug 1, 1995 |
| 0173-0933-10 | 90 TABLET, FILM COATED in 1 BOTTLE (0173-0933-10) | Aug 1, 1995 |
Other Valtrex products
- 0173-0565 Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · GlaxoSmithKline LLC
- 70518-2039 Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · REMEDYREPACK INC.