NDC 72789-263 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC72789-263

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
PD-Rx Pharmaceuticals, Inc.
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 (5)

Package NDCDescriptionSince
72789-263-066 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-06)Jun 18, 2025
72789-263-1010 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-10)Oct 11, 2022
72789-263-1414 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-14)Dec 4, 2023
72789-263-2828 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-28)Mar 3, 2025
72789-263-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-263-90)Jul 20, 2022

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