Valacyclovir Hydrochloride

Product NDC

51655-955

11-digit product format

516550955

Labeler code

51655

Product ID

51655-955_acafa40e-1f06-427b-91e6-eddc3caf162a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Northwind Pharmaceuticals

Application

ANDA090370

Marketing category

ANDA

Marketing start

2014-05-06

Marketing end

0000-00-00

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

E

Listing certified through

2018-12-31

Current FDA listing

Historical FDA.report record