Acyclovir

Product NDC

63629-1676

11-digit product format

636291676

Labeler code

63629

Product ID

63629-1676_ec58af2d-1415-47a2-b03f-4af2001e6134

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA074578

Marketing category

ANDA

Marketing start

1997-04-23

Marketing end

0000-00-00

Substance

ACYCLOVIR

Active strength

200 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

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record