NDC 68788-8820 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC68788-8820

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090682
Marketed since
January 23, 2025
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 Hydrochloride →

Package NDC codes (7)

Package NDCDescriptionSince
68788-8820-06 TABLET, FILM COATED in 1 BOTTLE (68788-8820-0)Jan 23, 2025
68788-8820-110 TABLET, FILM COATED in 1 BOTTLE (68788-8820-1)Jan 23, 2025
68788-8820-220 TABLET, FILM COATED in 1 BOTTLE (68788-8820-2)Jan 23, 2025
68788-8820-330 TABLET, FILM COATED in 1 BOTTLE (68788-8820-3)Jan 23, 2025
68788-8820-44 TABLET, FILM COATED in 1 BOTTLE (68788-8820-4)Jan 23, 2025
68788-8820-515 TABLET, FILM COATED in 1 BOTTLE (68788-8820-5)Jan 23, 2025
68788-8820-721 TABLET, FILM COATED in 1 BOTTLE (68788-8820-7)Jan 23, 2025

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