NDC 71335-1222 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1222

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA210401
Marketed since
May 4, 2018
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
71335-1222-0500 TABLET in 1 BOTTLE (71335-1222-0)Jan 30, 2025
71335-1222-125 TABLET in 1 BOTTLE (71335-1222-1)Jun 7, 2019
71335-1222-235 TABLET in 1 BOTTLE (71335-1222-2)Jun 3, 2019
71335-1222-330 TABLET in 1 BOTTLE (71335-1222-3)May 13, 2019
71335-1222-460 TABLET in 1 BOTTLE (71335-1222-4)Jan 30, 2025
71335-1222-550 TABLET in 1 BOTTLE (71335-1222-5)May 6, 2019
71335-1222-610 TABLET in 1 BOTTLE (71335-1222-6)Jan 30, 2025
71335-1222-740 TABLET in 1 BOTTLE (71335-1222-7)May 23, 2019
71335-1222-821 TABLET in 1 BOTTLE (71335-1222-8)Jan 30, 2025
71335-1222-990 TABLET in 1 BOTTLE (71335-1222-9)Jan 30, 2025

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