NDC 51655-703 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC51655-703

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090682
Marketed since
April 3, 2023
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
51655-703-044 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-04)Aug 15, 2023
51655-703-2121 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-21)Apr 3, 2023
51655-703-5310 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-703-53)Jun 15, 2023

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