NDC 31722-778 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC31722-778

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203834
Marketed since
November 29, 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
31722-778-01100 TABLET in 1 BOTTLE (31722-778-01)Nov 29, 2013
31722-778-05500 TABLET in 1 BOTTLE (31722-778-05)Nov 29, 2013

Recalls mentioning this NDC

Other Acyclovir products