NDC 71205-371 – Acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-371

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074891
Marketed since
August 8, 2013
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 (4)

Package NDCDescriptionSince
71205-371-3030 TABLET in 1 BOTTLE (71205-371-30)Feb 8, 2022
71205-371-3535 TABLET in 1 BOTTLE (71205-371-35)Feb 8, 2022
71205-371-6060 TABLET in 1 BOTTLE (71205-371-60)Feb 8, 2022
71205-371-9090 TABLET in 1 BOTTLE (71205-371-90)Feb 8, 2022

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