acyclovir

Product NDC

68071-4559

11-digit product format

680714559

Labeler code

68071

Product ID

68071-4559_75c289b3-09f7-7212-e053-2a91aa0a0ded

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

acyclovir

Dosage form

TABLET

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA204314

Marketing category

ANDA

Marketing start

2014-09-10

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

2020-12-31

Current FDA listing

Historical FDA.report record