NDC 68788-7587 – Valacyclovir

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

Human Prescription Drug

Product NDC68788-7587

Product details

Brand name
Valacyclovir
Generic name
Valacyclovir
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203047
Marketed since
May 25, 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 (7)

Package NDCDescriptionSince
68788-7587-06 TABLET, FILM COATED in 1 BOTTLE (68788-7587-0)Dec 27, 2019
68788-7587-110 TABLET, FILM COATED in 1 BOTTLE (68788-7587-1)Dec 27, 2019
68788-7587-220 TABLET, FILM COATED in 1 BOTTLE (68788-7587-2)Dec 27, 2019
68788-7587-330 TABLET, FILM COATED in 1 BOTTLE (68788-7587-3)Dec 27, 2019
68788-7587-44 TABLET, FILM COATED in 1 BOTTLE (68788-7587-4)Dec 27, 2019
68788-7587-515 TABLET, FILM COATED in 1 BOTTLE (68788-7587-5)Dec 27, 2019
68788-7587-721 TABLET, FILM COATED in 1 BOTTLE (68788-7587-7)Dec 27, 2019

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