Acyclovir

Product NDC

58118-8943

11-digit product format

581188943

Labeler code

58118

Product ID

58118-8943_8d8169f4-9b6d-569e-e053-2995a90aa5bf

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Clinical Solutions Wholesale

Application

ANDA074556

Marketing category

ANDA

Marketing start

1997-04-23

Marketing end

2019-11-01

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

0000-00-00

Current FDA listing

Historical FDA.report record