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ACYCLOVIR

NDC 70518-4186 · REMEDYREPACK INC.

Generic nameACYCLOVIR
Dosage formTABLET
RouteORAL
Active ingredient(s)ACYCLOVIR
Strength800 mg/1
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

70518-4186-0 — 10 TABLET in 1 BOTTLE, PLASTIC (70518-4186-0)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-138 — Acyclovir, 69452-290 — Acyclovir, 69452-291 — Acyclovir, 70518-0427 — acyclovir, 70518-1363 — acyclovir, 70518-1614 — acyclovir, 70518-2117 — Acyclovir, 70518-2455 — Acyclovir, 70518-2518 — Acyclovir, 70518-3436 — acyclovir, 70518-4414 — Acyclovir, 70518-4450 — Acyclovir, 70700-107 — Acyclovir, 70771-1371 — acyclovir, 70771-1808 — Acyclovir, 70954-188 — acyclovir, 71205-053 — Acyclovir, 71205-056 — Acyclovir, 71205-209 — Acyclovir, 71205-243 — ACYCLOVIR, +172 more

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