Class II · Moderate risk
Sofosbuvir and Velpatasvir
Defective Container: blister packs not properly sealed resulting in tablets being loose in the carton.
National Drug Code
Is NDC 72626-2701-01 recalled?
Sofosbuvir and Velpatasvir · 2 BLISTER PACK in 1 CARTON (72626-2701-1) / 14 TABLET, FILM COATED in 1 BLISTER PACK
Yes — this exact package was recalled
1 FDA recall names the code 72626-2701-01 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- Velpatasvir and Sofosbuvir
- Strength
- VELPATASVIR 100 mg/1; SOFOSBUVIR 400 mg/1
- Form
- Tablet, Film Coated · Oral
- Labeler
- Asegua Therapeutics LLC
- Type
- Human Prescription Drug
- Product code
- 72626-2701
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
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