Famciclovir

Product NDC

42291-275

11-digit product format

422910275

Labeler code

42291

Product ID

42291-275_9c5c0609-a5c8-b264-e053-2995a90a2c32

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Famciclovir

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA077487

Marketing category

ANDA

Marketing start

2012-01-04

Marketing end

0000-00-00

Substance

FAMCICLOVIR

Active strength

125 mg/1

Pharmacologic classes

DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record