Acyclovir

Product NDC

40085-842

11-digit product format

400850842

Labeler code

40085

Product ID

40085-842_418267ef-8fd5-4dc5-8d79-341805a8ee7c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

SUSPENSION

Route

ORAL

Labeler

Renaissance Pharma, Inc.

Application

NDA019909

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2014-09-03

Marketing end

2020-01-31

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