Testosterone Cypionate
Product Images NDC 0517-1830

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Testosterone Cypionate (NDC 0517-1830). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Testosterone Cypionate Injection Usp 1)

Chemical structure of Testosterone Cypionate illustrating its steroid backbone with specific functional groups, including a cyclopentylpropionate side chain.*

FDA Label Image

1 mL Container Label (Testosterone Cypionate Injection Usp 2)

Label for Testosterone Cypionate Injection, USP, 200 mg/mL, a 1 mL single-dose vial for intramuscular use. The label includes instructions to warm and shake the vial to redissolve any crystals that may have formed during storage at lower temperatures. It is labeled Rx Only and manufactured by American Regent, Inc.*

FDA Label Image

Carton Labeling (1 mL)

Packaging label for Testosterone Cypionate Injection, USP 200 mg/mL by American Regent, Inc. The label indicates it is for intramuscular use only, supplied as a 1 mL single-dose vial. The label includes storage instructions, dosage form, ingredient details, and a barcode, with the NDC 0517-1830-01 visible.*

FDA Label Image

Serialization Label (1 mL) (Testosterone Cypionate Injection Usp 4)

A label showing lot number and expiration date details for Testosterone Cypionate by American Regent, Inc. The lot number is "TEST" and the expiration date is November 2020. Additional printed codes include a GTIN and serial number, with a small square barcode visible on the left.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.