NDC 71335-1862 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · Oral
Product NDC71335-1862
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- Bryant Ranch Prepack
- 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
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1862-0 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1862-0) | Oct 21, 2021 |
| 71335-1862-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1862-1) | Oct 21, 2021 |
| 71335-1862-2 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-1862-2) | Oct 21, 2021 |
| 71335-1862-3 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1862-3) | Oct 21, 2021 |
| 71335-1862-4 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-1862-4) | Oct 21, 2021 |
| 71335-1862-5 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1862-5) | Oct 21, 2021 |
| 71335-1862-6 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-1862-6) | Oct 21, 2021 |
| 71335-1862-7 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1862-7) | Oct 21, 2021 |
| 71335-1862-8 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-1862-8) | Oct 21, 2021 |
| 71335-1862-9 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1862-9) | Oct 21, 2021 |
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