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Famciclovir

NDC 64980-349 · Rising Pharma Holdings, Inc.

Generic nameFamciclovir

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)FAMCICLOVIR

Strength125 mg/1

Pharmacologic classDNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]

Marketing categoryANDA

Packages

64980-349-03 — 30 TABLET, FILM COATED in 1 BOTTLE (64980-349-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-708 — Famciclovir, 33342-024 — Famciclovir, 33342-025 — Famciclovir, 33342-026 — Famciclovir, 42291-414 — Famciclovir, 42291-415 — Famciclovir, 42291-416 — Famciclovir, 55289-168 — Famciclovir, 63187-998 — Famciclovir, 63629-7890 — Famciclovir, 64980-350 — Famciclovir, 64980-351 — Famciclovir, 65862-465 — Famciclovir, 65862-466 — Famciclovir, 65862-467 — Famciclovir, 71205-609 — Famciclovir, 71335-2936 — Famciclovir, 73190-091 — Famciclovir, 73190-092 — Famciclovir, 73190-093 — Famciclovir, +5 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