NDC 23155-227 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC23155-227

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074891
Marketed since
August 8, 2013
Listing expires
December 31, 2027
Pharmacologic class
Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor; Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Acyclovir →

Package NDC codes (2)

Package NDCDescriptionSince
23155-227-01100 TABLET in 1 BOTTLE (23155-227-01)Aug 8, 2013
23155-227-05500 TABLET in 1 BOTTLE (23155-227-05)Aug 8, 2013

Recalls mentioning this NDC

Other Acyclovir products