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

Is NDC 59762-5008-01 recalled?

misoprostol · 60 TABLET in 1 BOTTLE (59762-5008-1)

Yes — this exact package was recalled

1 FDA recall names the code 59762-5008-01 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
Misoprostol
Strength
MISOPROSTOL 200 ug/1
Form
Tablet · Oral
Labeler
Mylan Pharmaceuticals Inc.
Type
Human Prescription Drug
Product code
59762-5008

Recalls naming this package

Class II ยท Moderate risk

Misoprostol

Labeling:Label Mixup; MISOPROSTOL Tablet, 200 mcg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: AD21790_34, EXP: 5/1/2014; SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: W003115, EXP: 6/13/2014.

Terminated Labeling / mix-up Aidapak Services, LLC D-649-2014

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