NDC 71335-1341 – Valacyclovir Hydrochloride

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

Human Prescription Drug

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

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1341-060 TABLET, FILM COATED in 1 BOTTLE (71335-1341-0)Nov 8, 2019
71335-1341-115 TABLET, FILM COATED in 1 BOTTLE (71335-1341-1)Apr 23, 2021
71335-1341-210 TABLET, FILM COATED in 1 BOTTLE (71335-1341-2)Sep 13, 2019
71335-1341-34 TABLET, FILM COATED in 1 BOTTLE (71335-1341-3)Dec 28, 2021
71335-1341-47 TABLET, FILM COATED in 1 BOTTLE (71335-1341-4)Sep 4, 2020
71335-1341-520 TABLET, FILM COATED in 1 BOTTLE (71335-1341-5)May 22, 2020
71335-1341-630 TABLET, FILM COATED in 1 BOTTLE (71335-1341-6)Sep 12, 2019
71335-1341-78 TABLET, FILM COATED in 1 BOTTLE (71335-1341-7)Jan 16, 2020
71335-1341-890 TABLET, FILM COATED in 1 BOTTLE (71335-1341-8)Dec 28, 2021
71335-1341-914 TABLET, FILM COATED in 1 BOTTLE (71335-1341-9)Feb 4, 2020

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