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

Is NDC 0591-0398-60 recalled?

Diclofenac Sodium and Misoprostol · 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (0591-0398-60)

Yes — this exact package was recalled

5 FDA recalls name the code 0591-0398-60 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
Diclofenac Sodium and Misoprostol
Strength
DICLOFENAC SODIUM 75 mg/1; MISOPROSTOL 200 ug/1
Form
Tablet, Delayed Release · Oral
Labeler
Actavis Pharma, Inc.
Type
Human Prescription Drug
Product code
0591-0398

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.

Other recalled products from this labeler