Acyclovir

Product NDC

0440-6030

11-digit product format

004406030

Labeler code

0440

Product ID

0440-6030_efebe3d3-b01e-4623-b044-6e6a09dd26ba

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

Liberty Pharmaceuticals, Inc.

Application

ANDA206261

Marketing category

ANDA

Marketing start

2017-08-17

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

2020-12-31

Current FDA listing

Historical FDA.report record