Acyclovir

Product NDC

70518-0131

11-digit product format

705180131

Labeler code

70518

Product ID

70518-0131_81fa1903-33ee-2cfc-e053-2991aa0a1460

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Acyclovir

Dosage form

CAPSULE

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA075090

Marketing category

ANDA

Marketing start

2017-01-17

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