acyclovir

Product NDC

68788-7760

11-digit product format

687887760

Labeler code

68788

Product ID

68788-7760_129e0b26-a3d6-484f-a721-f41dec56bde7

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA077309

Marketing category

ANDA

Marketing start

2020-07-01

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

2023-12-31

Current FDA listing

Historical FDA.report record