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

Is NDC 62756-0015-40 recalled?

Testosterone Cypionate · 1 VIAL in 1 CARTON (62756-015-40) / 1 mL in 1 VIAL

Yes — this exact package was recalled

7 FDA recalls name the code 62756-0015-40 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
Testosterone Cypionate
Strength
TESTOSTERONE CYPIONATE 200 mg/mL
Form
Injection, Solution · Intramuscular
Labeler
Sun Pharmaceutical Industries, Inc.
Type
Human Prescription Drug · DEA CIII
Product code
62756-0015

Recalls naming this package

Class II · Moderate risk

Testosterone Cypionate Injection

CGMP Deviations: Manufacturing deviations were reported due to an abnormal appearance on parts of machinery.

Terminated cGMP deviation Sun Pharmaceutical Industries INC NDC 62756-015-40 D-1176-2022
Class II · Moderate risk

Testosterone Cypionate Injection

CGMP Deviations: lots made with same active pharmaceutical ingredient (API) as lots that were rejected due to manufacturing issues that could cause the product to be out of specification for impurities.

Terminated Impurity / degradation Sun Pharmaceutical Industries INC NDC 62756-015-40 D-1153-2022
Class II · Moderate risk

Testosterone Cypionate for Injection

cGMP Deviations; released lots were manufactured under similar manufacturing conditions to a previously rejected OOS Lot.

Terminated Failed specification Sun Pharmaceutical Industries, Inc. NDC 62756-015-40 D-0788-2020

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