NDC 72626-2701 – Sofosbuvir and Velpatasvir

Velpatasvir 100 mg/1; Sofosbuvir 400 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC72626-2701

Product details

Brand name
Sofosbuvir and Velpatasvir
Generic name
Velpatasvir and Sofosbuvir
Labeler
Asegua Therapeutics LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA208341
Marketed since
November 14, 2018
Listing expires
December 31, 2026
Pharmacologic class
Hepatitis C Virus NS5A Inhibitor; Hepatitis C Virus Nucleotide Analog NS5B Polymerase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Sofosbuvir and Velpatasvir →

Package NDC codes (1)

Package NDCDescriptionSince
72626-2701-12 BLISTER PACK in 1 CARTON (72626-2701-1) / 14 TABLET, FILM COATED in 1 BLISTER PACKNov 14, 2018

Recalls mentioning this NDC