NDC 71335-1645 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1645

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Bryant Ranch Prepack
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 (10)

Package NDCDescriptionSince
71335-1645-0120 TABLET in 1 BOTTLE (71335-1645-0)Jul 9, 2020
71335-1645-120 TABLET in 1 BOTTLE (71335-1645-1)Jul 2, 2020
71335-1645-228 TABLET in 1 BOTTLE (71335-1645-2)Jan 28, 2022
71335-1645-330 TABLET in 1 BOTTLE (71335-1645-3)Jun 25, 2020
71335-1645-450 TABLET in 1 BOTTLE (71335-1645-4)Jan 28, 2022
71335-1645-515 TABLET in 1 BOTTLE (71335-1645-5)Jan 28, 2022
71335-1645-660 TABLET in 1 BOTTLE (71335-1645-6)Sep 23, 2020
71335-1645-725 TABLET in 1 BOTTLE (71335-1645-7)Dec 18, 2020
71335-1645-810 TABLET in 1 BOTTLE (71335-1645-8)Dec 23, 2020
71335-1645-940 TABLET in 1 BOTTLE (71335-1645-9)Jan 28, 2022

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