NDC 72162-1735 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72162-1735

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 (7)

Package NDCDescriptionSince
72162-1735-1120 TABLET in 1 BOTTLE, PLASTIC (72162-1735-1)Sep 6, 2024
72162-1735-220 TABLET in 1 BOTTLE, PLASTIC (72162-1735-2)Sep 6, 2024
72162-1735-330 TABLET in 1 BOTTLE, PLASTIC (72162-1735-3)Aug 15, 2024
72162-1735-428 TABLET in 1 BOTTLE, PLASTIC (72162-1735-4)Sep 6, 2024
72162-1735-510 TABLET in 1 BOTTLE, PLASTIC (72162-1735-5)Sep 6, 2024
72162-1735-660 TABLET in 1 BOTTLE, PLASTIC (72162-1735-6)Sep 6, 2024
72162-1735-750 TABLET in 1 BOTTLE, PLASTIC (72162-1735-7)Sep 6, 2024

Other Acyclovir products