NDC 71335-2229 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2229

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075382
Marketed since
October 22, 2009
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 (2)

Package NDCDescriptionSince
71335-2229-135 TABLET in 1 BOTTLE, PLASTIC (71335-2229-1)Sep 6, 2024
71335-2229-290 TABLET in 1 BOTTLE, PLASTIC (71335-2229-2)Aug 23, 2023

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