acyclovir

NDC 68788-4142 · c

Generic nameacyclovir

Dosage formOINTMENT

RouteTOPICAL

Active ingredient(s)ACYCLOVIR

Strength50 mg/g

Pharmacologic classDNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]

Marketing categoryANDA

Packages

68788-4142-1 — 15 g in 1 TUBE (68788-4142-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-2526 — Acyclovir, 68071-2811 — Acyclovir, 68071-3222 — Acyclovir, 68071-3573 — Acyclovir, 68071-3909 — acyclovir, 68071-4799 — Acyclovir, 68071-5100 — acyclovir, 68382-791 — acyclovir, 68382-792 — acyclovir, 68462-746 — acyclovir, 68788-7575 — Acyclovir, 68788-8203 — Acyclovir, 68788-8247 — acyclovir, 68788-8724 — Acyclovir, 68999-803 — Acyclovir, 69076-146 — Acyclovir, 69117-0018 — Acyclovir, 69117-0019 — Acyclovir, 69117-0039 — Acyclovir, 69367-137 — Acyclovir, +172 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels