NDC 52536-625
Testosterone Cypionate 200 mg per 1 mL injection
On the label: Wilshire Pharmaceuticals Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Wilshire Pharmaceuticals Inc. names for other drugs.
Recalls
- Feb 15, 2023 · Class II · Azurity Pharmaceuticals, Inc.
cGMP: complaints of crystals not redissolving into solution after warming and shaking the vials.
Lots: Lot #23804.034A, 23803.061A, Exp 9/2024 - Sep 27, 2019 · Class III · Arbor Pharmaceuticals Inc.
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
Lots: lot# 23803.002B, Exp 07/2020; 23803.005A, Exp 01/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Testosterone: every company that makes it
- Form
- injection, intramuscular
- Strength
- 200 mg per 1 mL
- Approval
- ANDA ANDA206368
- On the market since
- May 31, 2019
- Package NDCs
52536-625-0152536-625-10- Official label
- DailyMed (National Library of Medicine), updated Jul 24, 2025
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