Testosterone Cypionate Injection, Solution
Product Images NDC 62756-015

7 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Testosterone Cypionate (NDC 62756-015). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Testosterone-label-1000mg (Testosterone Label 1000mg)

Testosterone-label-1000mg (Testosterone Label 1000mg)
Label for Testosterone Cypionate Injection, USP, 100 mg/mL (1,000 mg/10 mL) in a 10 mL multiple-dose vial. The label provides storage instructions, lists benzyl benzoate, benzyl alcohol, and cottonseed oil as components, and states intramuscular use only. Distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharmaceutical Industries Ltd. in India.*
FDA Label Image

Testosterone-label-2000mg (Testosterone Label 2000mg)

Testosterone-label-2000mg (Testosterone Label 2000mg)
Label of Testosterone Cypionate Injection, USP 200 mg/mL (2,000 mg/10 mL) in a 10 mL multiple-dose vial for intramuscular use only. The label notes ingredients, storage conditions (20° to 25°C), and shaking instructions. Distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharmaceutical Industries Ltd., India.*
FDA Label Image

Testosterone-label-200mg (Testosterone Label 200mg)

Testosterone-label-200mg (Testosterone Label 200mg)
Label for Testosterone Cypionate Injection USP, 200 mg/mL, a single-dose 1 mL vial for intramuscular use. The label indicates storage instructions and is distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharma Industries Ltd., India. The NDC code is 62756-015-40.*
FDA Label Image

Testosterone-showbox-1000mg (Testosterone Showbox 1000mg)

Testosterone-showbox-1000mg (Testosterone Showbox 1000mg)
Packaging label for Testosterone Cypionate Injection, USP 100 mg/mL (1,000 mg/10 mL) by Sun Pharmaceutical Industries, Inc. The label details the intramuscular injection, highlights active ingredient concentration, storage instructions, and includes the NDC 62756-017-40. It also shows that it is a multiple-dose vial for prescription use only.*
FDA Label Image

Testosterone-showbox-2000mg (Testosterone Showbox 2000mg)

Testosterone-showbox-2000mg (Testosterone Showbox 2000mg)
Packaging label for Testosterone Cypionate Injection, USP 200 mg/mL (2,000 mg/10 mL) by Sun Pharmaceutical Industries, Inc. The image shows a multi-dose vial with intramuscular use only, Rx only, including storage instructions and inactive ingredients. The label features the NDC 62756-016-40 and highlights the drug strength in a purple box.*
FDA Label Image

Testosterone-showbox-200mg (Testosterone Showbox 200mg)

Testosterone-showbox-200mg (Testosterone Showbox 200mg)
The packaging label for Testosterone Cypionate Injection, USP 200 mg/mL by Sun Pharmaceutical Industries, Inc. The label indicates it is for intramuscular use only and is supplied as a 1 mL single-dose vial. The NDC is 62756-015-40. The label includes usage instructions for shaking the vial and storage conditions (20° to 25°C). Manufacturer and distributor information is also present.*
FDA Label Image

Chemical-structure (Testosterone Str)

Chemical-structure (Testosterone Str)
Chemical structure of Testosterone Cypionate showing the steroid backbone with functional groups including a ketone and cypionate ester side chain.*

* 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.