Acyclovir

Product NDC

17856-0082

11-digit product format

178560082

Labeler code

17856

Product ID

17856-0082_8d29b196-b71a-4252-a92a-0100a63ae43f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

SUSPENSION

Route

ORAL

Labeler

Atlantic Biologicals Corps

Application

ANDA077026

Marketing category

ANDA

Marketing start

2005-06-07

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

2020-12-31

Current FDA listing

Historical FDA.report record