Acyclovir

Product NDC

68788-9783

11-digit product format

687889783

Labeler code

68788

Product ID

68788-9783_7dee3511-8486-43e9-bf04-e6d1f41dffa7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

SUSPENSION

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA074738

Marketing category

ANDA

Marketing start

2012-07-27

Marketing end

0000-00-00

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

2019-12-31

Current FDA listing

Historical FDA.report record