Acyclovir

Product NDC

50268-060

11-digit product format

502680060

Labeler code

50268

Product ID

50268-060_64b79597-ab9c-9147-e053-2a91aa0a205a

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

AvPAK

Application

ANDA075090

Marketing category

ANDA

Marketing start

2013-05-02

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

2020-12-31

Current FDA listing

Historical FDA.report record