NDC 61919-066 – Valacyclovir

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

Human Prescription Drug

Product NDC61919-066

Product details

Brand name
Valacyclovir
Generic name
Valacyclovir
Labeler
Direct Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA201506
Marketed since
January 1, 2015
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 →

Package NDC codes (2)

Package NDCDescriptionSince
61919-066-2020 TABLET, FILM COATED in 1 BOTTLE (61919-066-20)Jan 1, 2015
61919-066-6060 TABLET, FILM COATED in 1 BOTTLE (61919-066-60)Jan 1, 2015

Other Valacyclovir products