ACYCLOVIR

Product NDC

70934-532

11-digit product format

709340532

Labeler code

70934

Product ID

70934-532_a9cbbf46-74fe-6dea-e053-2995a90a683f

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

2020-02-17

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