Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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National Drug Code

Is NDC 49702-0228-13 recalled?

Tivicay · 30 TABLET, FILM COATED in 1 BOTTLE (49702-228-13)

Yes — this exact package was recalled

2 FDA recalls name the code 49702-0228-13 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
dolutegravir sodium
Strength
DOLUTEGRAVIR SODIUM 50 mg/1
Form
Tablet, Film Coated · Oral
Labeler
ViiV Healthcare Company
Type
Human Prescription Drug
Product code
49702-0228

Recalls naming this package

Class III · Low risk

Tivicay (dolutegravir)

Labeling: incorrect or missing lot and/or expiration date. An incorrect expiration date was printed on the product labeling with an expiration date of January 2027, whereas the correct expiration date is September 2026.

Terminated Labeling / mix-up GlaxoSmithKline LLC NDC 49702-228-13 D-0896-2022
Class III · Low risk

Tivicay (dolutegravir)

Cross Contamination with Other Products: Product contains Promacta (eltrombopag).

Terminated Cross-contamination Viiv Healthcare Company NDC 49702-228-13 D-1185-2014

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.

Other recalled products from this labeler