NDC 71335-0630 – Valacyclovir

Valacyclovir Hydrochloride 1 g/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-0630

Product details

Brand name
Valacyclovir
Generic name
Valacyclovir
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203047
Marketed since
May 25, 2015
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 →

Package NDC codes (10)

Package NDCDescriptionSince
71335-0630-060 TABLET, FILM COATED in 1 BOTTLE (71335-0630-0)Oct 5, 2021
71335-0630-130 TABLET, FILM COATED in 1 BOTTLE (71335-0630-1)May 29, 2018
71335-0630-221 TABLET, FILM COATED in 1 BOTTLE (71335-0630-2)Mar 21, 2018
71335-0630-320 TABLET, FILM COATED in 1 BOTTLE (71335-0630-3)Jul 24, 2018
71335-0630-44 TABLET, FILM COATED in 1 BOTTLE (71335-0630-4)Jul 13, 2018
71335-0630-510 TABLET, FILM COATED in 1 BOTTLE (71335-0630-5)May 28, 2019
71335-0630-66 TABLET, FILM COATED in 1 BOTTLE (71335-0630-6)Mar 20, 2018
71335-0630-715 TABLET, FILM COATED in 1 BOTTLE (71335-0630-7)Mar 4, 2019
71335-0630-88 TABLET, FILM COATED in 1 BOTTLE (71335-0630-8)May 29, 2018
71335-0630-990 TABLET, FILM COATED in 1 BOTTLE (71335-0630-9)Feb 18, 2020

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