NDC 85766-054 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC85766-054

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
Sportpharm LLC
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 (12)

Package NDCDescriptionSince
85766-054-01100 TABLET, FILM COATED in 1 BOTTLE (85766-054-01)Aug 17, 2025
85766-054-022 TABLET, FILM COATED in 1 BOTTLE (85766-054-02)Aug 17, 2025
85766-054-044 TABLET, FILM COATED in 1 BOTTLE (85766-054-04)Aug 17, 2025
85766-054-077 TABLET, FILM COATED in 1 BOTTLE (85766-054-07)Aug 17, 2025
85766-054-1010 TABLET, FILM COATED in 1 BOTTLE (85766-054-10)Aug 17, 2025
85766-054-1414 TABLET, FILM COATED in 1 BOTTLE (85766-054-14)Aug 17, 2025
85766-054-1515 TABLET, FILM COATED in 1 BOTTLE (85766-054-15)Aug 17, 2025
85766-054-2020 TABLET, FILM COATED in 1 BOTTLE (85766-054-20)Aug 17, 2025
85766-054-2828 TABLET, FILM COATED in 1 BOTTLE (85766-054-28)Oct 23, 2025
85766-054-3030 TABLET, FILM COATED in 1 BOTTLE (85766-054-30)Aug 17, 2025
85766-054-6060 TABLET, FILM COATED in 1 BOTTLE (85766-054-60)Aug 17, 2025
85766-054-9090 TABLET, FILM COATED in 1 BOTTLE (85766-054-90)Aug 17, 2025

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