NDC 0093-8118 – Famciclovir

Famciclovir 250 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-8118

Product details

Brand name
Famciclovir
Generic name
Famciclovir
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077487
Marketed since
September 5, 2007
Listing expires
December 31, 2026
Pharmacologic class
Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Famciclovir →

Package NDC codes (1)

Package NDCDescriptionSince
0093-8118-5630 TABLET, FILM COATED in 1 BOTTLE (0093-8118-56)Sep 5, 2007

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