NDC 71335-1341 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-1341
Product details
- Brand name
- Valacyclovir Hydrochloride
- Generic name
- Valacyclovir Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078518
- Marketed since
- May 24, 2010
- 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
Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-1341-0 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-1341-0) | Nov 8, 2019 |
| 71335-1341-1 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-1341-1) | Apr 23, 2021 |
| 71335-1341-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-1341-2) | Sep 13, 2019 |
| 71335-1341-3 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-1341-3) | Dec 28, 2021 |
| 71335-1341-4 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-1341-4) | Sep 4, 2020 |
| 71335-1341-5 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-1341-5) | May 22, 2020 |
| 71335-1341-6 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-1341-6) | Sep 12, 2019 |
| 71335-1341-7 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-1341-7) | Jan 16, 2020 |
| 71335-1341-8 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-1341-8) | Dec 28, 2021 |
| 71335-1341-9 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-1341-9) | Feb 4, 2020 |
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