NDC 71335-0708 – Valacyclovir Hydrochloride

Valacyclovir Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

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

Uses, dosage, side effects and warnings for Valacyclovir Hydrochloride →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0708-060 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)Feb 10, 2022
71335-0708-115 TABLET, FILM COATED in 1 BOTTLE (71335-0708-1)Jan 11, 2022
71335-0708-210 TABLET, FILM COATED in 1 BOTTLE (71335-0708-2)Apr 12, 2018
71335-0708-34 TABLET, FILM COATED in 1 BOTTLE (71335-0708-3)Apr 20, 2022
71335-0708-47 TABLET, FILM COATED in 1 BOTTLE (71335-0708-4)Apr 24, 2018
71335-0708-520 TABLET, FILM COATED in 1 BOTTLE (71335-0708-5)Oct 19, 2021
71335-0708-630 TABLET, FILM COATED in 1 BOTTLE (71335-0708-6)Feb 26, 2018
71335-0708-78 TABLET, FILM COATED in 1 BOTTLE (71335-0708-7)Aug 16, 2018
71335-0708-890 TABLET, FILM COATED in 1 BOTTLE (71335-0708-8)Jun 14, 2019
71335-0708-914 TABLET, FILM COATED in 1 BOTTLE (71335-0708-9)Apr 22, 2019

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