Class II · Moderate risk
Testosterone Cypionate Injection
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
National Drug Code
Is NDC 52536-0625-01 recalled?
Testosterone Cypionate · 1 VIAL, SINGLE-DOSE in 1 CARTON (52536-625-01) / 1 mL in 1 VIAL, SINGLE-DOSE
Yes — this exact package was recalled
2 FDA recalls name the code 52536-0625-01 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
- testosterone cypionate
- Strength
- TESTOSTERONE CYPIONATE 200 mg/mL
- Form
- Injection · Intramuscular
- Labeler
- Wilshire Pharmaceuticals
- Type
- Human Prescription Drug · DEA CIII
- Product code
- 52536-0625
Recalls naming this package
Class III · Low risk
Testosterone Cypionate Injection
Labeling:Label Mix-up: Shipper Carton labelled Testosterone Cypionate Injection, USP, 200mg/mL, 1 ml single-dose vials, found to contain shelf cartons labelled as Testosterone Cypionate Injection USP, 200mg/mL, 10 ml multi-dose vials which contain Testosterone Cypionate Injection USP, 200mg/mL,1mL single-does vials
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
- 52536-0129 See recall 1
- 52536-0133 See recall 1
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