NDC 68788-8820 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · Oral
Product NDC68788-8820
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- January 23, 2025
- Listing expires
- December 31, 2026
- 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
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8820-0 | 6 TABLET, FILM COATED in 1 BOTTLE (68788-8820-0) | Jan 23, 2025 |
| 68788-8820-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68788-8820-1) | Jan 23, 2025 |
| 68788-8820-2 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-8820-2) | Jan 23, 2025 |
| 68788-8820-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8820-3) | Jan 23, 2025 |
| 68788-8820-4 | 4 TABLET, FILM COATED in 1 BOTTLE (68788-8820-4) | Jan 23, 2025 |
| 68788-8820-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-8820-5) | Jan 23, 2025 |
| 68788-8820-7 | 21 TABLET, FILM COATED in 1 BOTTLE (68788-8820-7) | Jan 23, 2025 |
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