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

Is NDC 57664-0051-88 recalled?

Lisdexamfetamine Dimesylate · 100 CAPSULE in 1 BOTTLE (57664-051-88)

Yes — this exact package was recalled

2 FDA recalls name the code 57664-0051-88 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.

2 of these recalls are still ongoing.

Active ingredient
Lisdexamfetamine Dimesylate
Strength
LISDEXAMFETAMINE DIMESYLATE 60 mg/1
Form
Capsule · Oral
Labeler
Sun Pharmaceutical Industries, Inc.
Type
Human Prescription Drug · DEA CII
Product code
57664-0051

Recalls naming this package

Class II · Moderate risk

Lisdexamfetamine Dimesylate Capsules

Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 12-month long term stability station (25¿C, 60%RH) for Lisdexamfetamine dimesylate capsules.

Ongoing Dissolution failure Sun Pharmaceutical Industries INC NDC 57664-051-88 D-0149-2026
Class II · Moderate risk

Lisdexamfetamine Dimesylate Capsules

Failed Dissolution Specifications: An out of specification results observed in dissolution test during analysis at 9 month long term stability station (25¿C, 60%RH).

Ongoing Dissolution failure Sun Pharmaceutical Industries INC NDC 57664-051-88 D-0516-2025

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