NDC 70518-0541 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC70518-0541

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078518
Marketed since
May 15, 2017
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 (5)

Package NDCDescriptionSince
70518-0541-114 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-1)Sep 29, 2025
70518-0541-25 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-2)Sep 29, 2025
70518-0541-320 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-3)Oct 3, 2025
70518-0541-44 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-4)Oct 30, 2025
70518-0541-55 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0541-5)Oct 30, 2025

Other Valacyclovir Hydrochloride products