Acyclovir

Product NDC

42708-073

11-digit product format

427080073

Labeler code

42708

Product ID

42708-073_e0f38890-5f9c-43ab-9f81-527fb42e39ce

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

QPharma Inc

Application

ANDA074556

Marketing category

ANDA

Marketing start

1997-04-23

Marketing end

0000-00-00

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

2020-12-31

Current FDA listing

Historical FDA.report record