NDC 71335-0708 – Valacyclovir Hydrochloride
Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0708
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, 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 |
|---|---|---|
| 71335-0708-0 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0) | Feb 10, 2022 |
| 71335-0708-1 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1) | Jan 11, 2022 |
| 71335-0708-2 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2) | Apr 12, 2018 |
| 71335-0708-3 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3) | Apr 20, 2022 |
| 71335-0708-4 | 7 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4) | Apr 24, 2018 |
| 71335-0708-5 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5) | Oct 19, 2021 |
| 71335-0708-6 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6) | Feb 26, 2018 |
| 71335-0708-7 | 8 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7) | Aug 16, 2018 |
| 71335-0708-8 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8) | Jun 14, 2019 |
| 71335-0708-9 | 14 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9) | Apr 22, 2019 |
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