NDC 63629-1678 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC63629-1678

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
63629-1678-0500 TABLET in 1 BOTTLE (63629-1678-0)May 21, 2018
63629-1678-125 TABLET in 1 BOTTLE (63629-1678-1)Oct 29, 2024
63629-1678-235 TABLET in 1 BOTTLE (63629-1678-2)Oct 29, 2024
63629-1678-330 TABLET in 1 BOTTLE (63629-1678-3)Oct 29, 2024
63629-1678-460 TABLET in 1 BOTTLE (63629-1678-4)Oct 29, 2024
63629-1678-550 TABLET in 1 BOTTLE (63629-1678-5)Oct 29, 2024
63629-1678-610 TABLET in 1 BOTTLE (63629-1678-6)Mar 28, 2013
63629-1678-740 TABLET in 1 BOTTLE (63629-1678-7)Jun 9, 2011
63629-1678-821 TABLET in 1 BOTTLE (63629-1678-8)Nov 17, 2011
63629-1678-990 TABLET in 1 BOTTLE (63629-1678-9)Jun 4, 2020

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