NDC 70518-3359 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC70518-3359

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090682
Marketed since
February 7, 2022
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 (3)

Package NDCDescriptionSince
70518-3359-121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-1)Feb 14, 2022
70518-3359-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-2)Oct 14, 2025
70518-3359-314 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3359-3)Feb 18, 2026

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