ACYCLOVIR

Product NDC

70934-511

11-digit product format

709340511

Labeler code

70934

Product ID

70934-511_a14042bf-5316-11c0-e053-2a95a90aca1b

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ACYCLOVIR

Dosage form

TABLET

Route

ORAL

Labeler

Denton Pharma, Inc. DBA Northwind Pharmaceuticals

Application

ANDA074891

Marketing category

ANDA

Marketing start

2020-01-28

Marketing end

0000-00-00

Substance

ACYCLOVIR

Active strength

800 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

2021-12-31

Current FDA listing

Historical FDA.report record