Valacyclovir hydrochloride

Product NDC

68788-6345

11-digit product format

687886345

Labeler code

68788

Product ID

68788-6345_2180c750-695b-4730-b928-daca1d88a2b5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA077135

Marketing category

ANDA

Marketing start

2016-10-24

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

2022-12-31

Current FDA listing

Historical FDA.report record