Acyclovir

Product NDC

50090-2382

11-digit product format

500902382

Labeler code

50090

Product ID

50090-2382_2f4ff373-0127-4933-ac0e-0e5d1b539a48

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA075382

Marketing category

ANDA

Marketing start

2009-10-22

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

2019-12-31

Current FDA listing

Historical FDA.report record