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

Is NDC 0078-0972-61 recalled?

Promacta · 1 CARTON in 1 KIT (0078-0972-61) / 30 PACKET in 1 CARTON (0078-0972-23) / 1 POWDER, FOR SUSPENSION in 1 PACKET (0078-0972-19)

Yes — this exact package was recalled

1 FDA recall names the code 0078-0972-61 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
eltrombopag olamine
Strength
ELTROMBOPAG OLAMINE 12.5 mg/1
Form
Powder, for Suspension · Oral
Labeler
Novartis Pharmaceuticals Corporation
Type
Human Prescription Drug
Product code
0078-0972

Recalls naming this package

Class I ยท High risk

Promacta (eltrombopag)

Cross Contamination with Other Products: product is being recalled due to possible cross-contamination with peanut flour.

Terminated Cross-contamination Novartis Pharmaceuticals Corp. NDC 0078-0972-61 D-1309-2019

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