NDC 71205-388 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-388

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074891
Marketed since
August 8, 2013
Listing expires
December 31, 2026
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 (4)

Package NDCDescriptionSince
71205-388-3030 TABLET in 1 BOTTLE (71205-388-30)Feb 8, 2022
71205-388-3535 TABLET in 1 BOTTLE (71205-388-35)Feb 8, 2022
71205-388-6060 TABLET in 1 BOTTLE (71205-388-60)Feb 8, 2022
71205-388-9090 TABLET in 1 BOTTLE (71205-388-90)Feb 8, 2022

Other Acyclovir products