Acyclovir

Product NDC

55289-629

11-digit product format

552890629

Labeler code

55289

Product ID

55289-629_7bbf3721-b253-8650-e053-2a91aa0a7449

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

PD-Rx Pharmaceuticals, Inc.

Application

ANDA074556

Marketing category

ANDA

Marketing start

1997-04-30

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

2019-12-31

Current FDA listing

Historical FDA.report record