NDC 65862-449 – Valacyclovir Hydrochloride

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

Human Prescription Drug

Product NDC65862-449

Product details

Brand name
Valacyclovir Hydrochloride
Generic name
Valacyclovir Hydrochloride
Labeler
Aurobindo Pharma Limited
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 (5)

Package NDCDescriptionSince
65862-449-01100 TABLET, FILM COATED in 1 BOTTLE (65862-449-01)May 24, 2010
65862-449-05500 TABLET, FILM COATED in 1 BOTTLE (65862-449-05)May 24, 2010
65862-449-151500 TABLET, FILM COATED in 1 BOTTLE (65862-449-15)May 24, 2010
65862-449-3030 TABLET, FILM COATED in 1 BOTTLE (65862-449-30)May 24, 2010
65862-449-9090 TABLET, FILM COATED in 1 BOTTLE (65862-449-90)May 24, 2010

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