Valacyclovir Hydrochloride

Product NDC

55154-6837

11-digit product format

551546837

Labeler code

55154

Product ID

55154-6837_3aa7d81a-b8b5-462f-9322-a05e64b43ebd

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Cardinal Health

Application

ANDA090682

Marketing category

ANDA

Marketing start

2011-05-23

Marketing end

2020-12-31

Substance

VALACYCLOVIR HYDROCHLORIDE

Active strength

500 mg/1

Pharmacologic classes

DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record