Acyclovir

NDC 71335-1222 · Bryant Ranch Prepack

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

71335-1222-0 500 TABLET in 1 BOTTLE (71335-1222-0)

71335-1222-1 25 TABLET in 1 BOTTLE (71335-1222-1)

71335-1222-2 35 TABLET in 1 BOTTLE (71335-1222-2)

71335-1222-3 30 TABLET in 1 BOTTLE (71335-1222-3)

71335-1222-4 60 TABLET in 1 BOTTLE (71335-1222-4)

71335-1222-5 50 TABLET in 1 BOTTLE (71335-1222-5)

71335-1222-6 10 TABLET in 1 BOTTLE (71335-1222-6)

71335-1222-7 40 TABLET in 1 BOTTLE (71335-1222-7)

71335-1222-8 21 TABLET in 1 BOTTLE (71335-1222-8)

71335-1222-9 90 TABLET in 1 BOTTLE (71335-1222-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-472 — Acyclovir, 71205-578 — Acyclovir, 71209-004 — Acyclovir, 71209-005 — Acyclovir, 71209-006 — Acyclovir, 71335-0280 — Acyclovir, 71335-0323 — Acyclovir, 71335-0470 — ACYCLOVIR, 71335-0695 — Acyclovir, 71335-1053 — Acyclovir, 71335-1290 — Acyclovir, 71335-1381 — acyclovir, 71335-1645 — ACYCLOVIR, 71335-1757 — ACYCLOVIR, 71335-2229 — Acyclovir, 71335-2261 — acyclovir, 71335-2555 — Acyclovir, 71335-2619 — Acyclovir, 71335-3103 — Acyclovir, 71335-9620 — 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.