acyclovir

Product NDC

63629-1192

11-digit product format

636291192

Labeler code

63629

Product ID

63629-1192_43532e73-a33e-46e5-a9f4-cd0e9ee6a2e2

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA077309

Marketing category

ANDA

Marketing start

2006-03-13

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

2022-12-31

Current FDA listing

Historical FDA.report record