Valacyclovir

Product NDC

70518-0323

11-digit product format

705180323

Labeler code

70518

Product ID

70518-0323_839be353-4cd5-5b75-e053-2991aa0a9239

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA076588

Marketing category

ANDA

Marketing start

2017-03-16

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

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record