Acyclovir

Product NDC

68788-7342

11-digit product format

687887342

Labeler code

68788

Product ID

68788-7342_68cd26ca-890f-406e-b308-03110808e08e

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA210401

Marketing category

ANDA

Marketing start

2019-03-11

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