NDC 71205-391 – acyclovir

Acyclovir 400 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-391

Product details

Brand name
acyclovir
Generic name
acyclovir
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077309
Marketed since
June 9, 2007
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
71205-391-2525 TABLET in 1 BOTTLE (71205-391-25)Jan 28, 2020
71205-391-3030 TABLET in 1 BOTTLE (71205-391-30)Jan 28, 2020
71205-391-6060 TABLET in 1 BOTTLE (71205-391-60)Jan 28, 2020
71205-391-9090 TABLET in 1 BOTTLE (71205-391-90)Jan 28, 2020

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