VALACYCLOVIR HYDROCHLORIDE

Product NDC

68788-9554

11-digit product format

687889554

Labeler code

68788

Product ID

68788-9554_544f9814-0cf5-40d4-ab99-e28ac9a6d325

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

VALACYCLOVIR HYDROCHLORIDE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA090216

Marketing category

ANDA

Marketing start

2013-10-03

Marketing end

0000-00-00

Substance

VALACYCLOVIR HYDROCHLORIDE

Active strength

1 g/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