NDC 68071-2738 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-2738
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- NuCare Pharmaceuticals,Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090682
- Marketed since
- May 24, 2010
- 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 500 mg/1
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68071-2738-1 | 10 TABLET, FILM COATED in 1 BOTTLE (68071-2738-1) | May 27, 2022 |
| 68071-2738-4 | 14 TABLET, FILM COATED in 1 BOTTLE (68071-2738-4) | May 27, 2022 |
| 68071-2738-6 | 6 TABLET, FILM COATED in 1 BOTTLE (68071-2738-6) | Nov 8, 2024 |
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