Acyclovir

Product NDC

70518-2032

11-digit product format

705182032

Labeler code

70518

Product ID

70518-2032_874dcc1a-65c1-8ecb-e053-2995a90a1ef0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA210401

Marketing category

ANDA

Marketing start

2019-04-19

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

2020-12-31

Current FDA listing

Historical FDA.report record