Acyclovir

Product NDC

68788-9690

11-digit product format

687889690

Labeler code

68788

Product ID

68788-9690_5337364e-bd0c-4747-9ad2-244c80a2aace

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA075090

Marketing category

ANDA

Marketing start

2013-03-26

Marketing end

0000-00-00

Substance

ACYCLOVIR

Active strength

200 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