NDC 70518-2266 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC70518-2266

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090682
Marketed since
August 15, 2019
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
70518-2266-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2266-0)Aug 15, 2019
70518-2266-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2266-1)May 26, 2021
70518-2266-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2266-2)Jul 6, 2021

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