NDC 63187-832 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC63187-832

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090682
Marketed since
May 24, 2010
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 Hydrochloride →

Package NDC codes (9)

Package NDCDescriptionSince
63187-832-044 TABLET, FILM COATED in 1 BOTTLE (63187-832-04)Apr 3, 2017
63187-832-066 TABLET, FILM COATED in 1 BOTTLE (63187-832-06)Apr 3, 2017
63187-832-1010 TABLET, FILM COATED in 1 BOTTLE (63187-832-10)Jul 2, 2018
63187-832-1414 TABLET, FILM COATED in 1 BOTTLE (63187-832-14)Apr 3, 2017
63187-832-2121 TABLET, FILM COATED in 1 BOTTLE (63187-832-21)Apr 3, 2017
63187-832-2828 TABLET, FILM COATED in 1 BOTTLE (63187-832-28)Apr 3, 2017
63187-832-3030 TABLET, FILM COATED in 1 BOTTLE (63187-832-30)Apr 3, 2017
63187-832-6060 TABLET, FILM COATED in 1 BOTTLE (63187-832-60)Apr 3, 2017
63187-832-9090 TABLET, FILM COATED in 1 BOTTLE (63187-832-90)Apr 3, 2017

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