Valacyclovir hydrochloride

Product NDC

70934-180

11-digit product format

709340180

Labeler code

70934

Product ID

70934-180_98fb5e97-3ac9-b4b6-e053-2995a90ab3ec

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Denton Pharma, Inc. DBA Northwind Pharmaceuticals

Application

ANDA077135

Marketing category

ANDA

Marketing start

2018-10-29

Marketing end

0000-00-00

Substance

VALACYCLOVIR HYDROCHLORIDE

Active strength

1000 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

2020-12-31

Current FDA listing

Historical FDA.report record