NDC 71335-9620 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9620

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA209366
Marketed since
August 15, 2020
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 (10)

Package NDCDescriptionSince
71335-9620-0120 TABLET in 1 BOTTLE (71335-9620-0)Apr 5, 2024
71335-9620-120 TABLET in 1 BOTTLE (71335-9620-1)Mar 27, 2023
71335-9620-228 TABLET in 1 BOTTLE (71335-9620-2)Apr 5, 2024
71335-9620-330 TABLET in 1 BOTTLE (71335-9620-3)Apr 5, 2024
71335-9620-450 TABLET in 1 BOTTLE (71335-9620-4)Apr 5, 2024
71335-9620-515 TABLET in 1 BOTTLE (71335-9620-5)Mar 21, 2023
71335-9620-660 TABLET in 1 BOTTLE (71335-9620-6)Apr 19, 2023
71335-9620-725 TABLET in 1 BOTTLE (71335-9620-7)Jan 3, 2023
71335-9620-810 TABLET in 1 BOTTLE (71335-9620-8)Apr 5, 2024
71335-9620-940 TABLET in 1 BOTTLE (71335-9620-9)Apr 5, 2024

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