Valacyclovir hydrochloride

Product NDC

50090-2101

11-digit product format

500902101

Labeler code

50090

Product ID

50090-2101_a487c289-51cf-4de4-9544-7f1fe39f8da6

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Valacyclovir hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

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

2019-12-31

Current FDA listing

Historical FDA.report record