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

Is NDC 27241-0255-01 recalled?

Fluphenazine hydrochloride · 100 TABLET in 1 BOTTLE (27241-255-01)

Yes — this exact package was recalled

1 FDA recall names the code 27241-0255-01 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.

1 of these recalls is still ongoing.

Active ingredient
Fluphenazine hydrochloride
Strength
FLUPHENAZINE HYDROCHLORIDE 1 mg/1
Form
Tablet · Oral
Labeler
Ajanta Pharma USA Inc.
Type
Human Prescription Drug
Product code
27241-0255

Recalls naming this package

Class III ยท Low risk

Fluphenazine Hydrochloride Tablets

Failed impurities/degradation specifications: (OOS) for Organic Impurities by HPLC (Impurity-A) during testing at the 18 months long term stability. Result: 1.1 percent. Spec: 1.0 percent.

Ongoing Impurity / degradation Ajanta Pharma USA Inc NDC 27241-255-01 D-0836-2026

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