ACYCLOVIR

Product NDC

68788-6827

11-digit product format

687886827

Labeler code

68788

Product ID

68788-6827_5363e037-70dc-4307-8d22-2b46aebd1d99

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

ACYCLOVIR

Dosage form

CAPSULE

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA075677

Marketing category

ANDA

Marketing start

2017-01-23

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record