Valacyclovir hydrochloride

Product NDC

68071-2110

11-digit product format

680712110

Labeler code

68071

Product ID

68071-2110_46e03120-8386-382a-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA077135

Marketing category

ANDA

Marketing start

2010-05-24

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

2020-12-31

Current FDA listing

Historical FDA.report record