NDC 71335-9721 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-9721

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 (10)

Package NDCDescriptionSince
71335-9721-0500 TABLET in 1 BOTTLE, PLASTIC (71335-9721-0)Sep 6, 2024
71335-9721-125 TABLET in 1 BOTTLE, PLASTIC (71335-9721-1)Sep 6, 2024
71335-9721-235 TABLET in 1 BOTTLE, PLASTIC (71335-9721-2)Sep 6, 2024
71335-9721-330 TABLET in 1 BOTTLE, PLASTIC (71335-9721-3)Sep 6, 2024
71335-9721-460 TABLET in 1 BOTTLE, PLASTIC (71335-9721-4)Sep 6, 2024
71335-9721-550 TABLET in 1 BOTTLE, PLASTIC (71335-9721-5)Sep 6, 2024
71335-9721-610 TABLET in 1 BOTTLE, PLASTIC (71335-9721-6)Sep 6, 2024
71335-9721-740 TABLET in 1 BOTTLE, PLASTIC (71335-9721-7)Sep 6, 2024
71335-9721-821 TABLET in 1 BOTTLE, PLASTIC (71335-9721-8)Sep 6, 2024
71335-9721-990 TABLET in 1 BOTTLE, PLASTIC (71335-9721-9)Sep 6, 2024

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