acyclovir

Product NDC

68788-8989

11-digit product format

687888989

Labeler code

68788

Product ID

68788-8989_23fc147d-0df8-4f63-ba32-924a1b759410

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA077309

Marketing category

ANDA

Marketing start

2016-02-01

Marketing end

0000-00-00

Substance

ACYCLOVIR

Active strength

800 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