NDC 68071-3222 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3222

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203834
Marketed since
November 29, 2013
Listing expires
December 31, 2027
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 (8)

Package NDCDescriptionSince
68071-3222-050 TABLET in 1 BOTTLE (68071-3222-0)Jun 8, 2017
68071-3222-121 TABLET in 1 BOTTLE (68071-3222-1)Jun 8, 2017
68071-3222-225 TABLET in 1 BOTTLE (68071-3222-2)Jun 8, 2017
68071-3222-330 TABLET in 1 BOTTLE (68071-3222-3)Jun 8, 2017
68071-3222-414 TABLET in 1 BOTTLE (68071-3222-4)Jun 8, 2017
68071-3222-535 TABLET in 1 BOTTLE (68071-3222-5)Jun 8, 2017
68071-3222-640 TABLET in 1 BOTTLE (68071-3222-6)Aug 27, 2026
68071-3222-715 TABLET in 1 BOTTLE (68071-3222-7)Jun 8, 2017

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