NDC 68071-2408 – Acyclovir

Acyclovir 800 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-2408

Product details

Brand name
Acyclovir
Generic name
Acyclovir
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA075382
Marketed since
October 22, 2009
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 (6)

Package NDCDescriptionSince
68071-2408-121 TABLET in 1 BOTTLE, PLASTIC (68071-2408-1)May 21, 2021
68071-2408-225 TABLET in 1 BOTTLE, PLASTIC (68071-2408-2)May 21, 2021
68071-2408-330 TABLET in 1 BOTTLE, PLASTIC (68071-2408-3)May 21, 2021
68071-2408-414 TABLET in 1 BOTTLE, PLASTIC (68071-2408-4)May 21, 2021
68071-2408-535 TABLET in 1 BOTTLE, PLASTIC (68071-2408-5)May 21, 2021
68071-2408-715 TABLET in 1 BOTTLE, PLASTIC (68071-2408-7)May 21, 2021

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