NDC 68788-8705 – Valacyclovir
Valacyclovir Hydrochloride 1000 mg/1 · Tablet · Oral
Product NDC68788-8705
Product details
- Brand name
- Valacyclovir
- Generic name
- Valacyclovir
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA209553
- Marketed since
- July 1, 2024
- 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
- Valacyclovir Hydrochloride 1000 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8705-0 | 6 TABLET in 1 BOTTLE (68788-8705-0) | Jul 1, 2024 |
| 68788-8705-1 | 10 TABLET in 1 BOTTLE (68788-8705-1) | Jul 1, 2024 |
| 68788-8705-2 | 20 TABLET in 1 BOTTLE (68788-8705-2) | Jul 1, 2024 |
| 68788-8705-3 | 30 TABLET in 1 BOTTLE (68788-8705-3) | Jul 1, 2024 |
| 68788-8705-4 | 4 TABLET in 1 BOTTLE (68788-8705-4) | Jul 1, 2024 |
| 68788-8705-5 | 15 TABLET in 1 BOTTLE (68788-8705-5) | Jul 1, 2024 |
| 68788-8705-7 | 21 TABLET in 1 BOTTLE (68788-8705-7) | Jul 1, 2024 |
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