Acyclovir

Product NDC

68788-7576

11-digit product format

687887576

Labeler code

68788

Product ID

68788-7576_48d1fa56-f874-4a27-aa63-9ca0c0a7af36

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA203834

Marketing category

ANDA

Marketing start

2013-11-29

Marketing end

0000-00-00

Substance

ACYCLOVIR

Active strength

400 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

2022-12-31

Current FDA listing

Historical FDA.report record