ZOVIRAX

Product NDC

40076-953

11-digit product format

400760953

Labeler code

40076

Product ID

40076-953_9e574cb0-de5c-47b0-91d3-044a7ad212d9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acyclovir

Dosage form

SUSPENSION

Route

ORAL

Labeler

Prestium Pharma, Inc.

Application

NDA019909

Marketing category

NDA

Marketing start

2014-02-07

Marketing end

2019-08-31

Substance

ACYCLOVIR

Active strength

200 mg/5mL

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

0000-00-00

Current FDA listing

Historical FDA.report record