Depo-testosterone Injection, Solution
Product Images NDC 0009-0086

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Depo-testosterone (NDC 0009-0086). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Pharmacia & Upjohn Company Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Depo 01)

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Logo (Depo 02)

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Principal Display Panel (10 mL Vial Label)

Depo-Testosterone is a prescription-only drug that contains Testosterone Cypionate for intramuscular use. It comes in a 10 mL Multiple-Dose Vial and has a strength of 100 mg/mL. The drug should only be used as prescribed by a healthcare professional. The manufacturer is Pharmacia & Upjohn Co., a division of Pfizer Inc. The drug is distributed under the trademark Novaplus.*

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Principal Display Panel (10 mL Vial Carton)

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Principal Display Panel (1 mL Vial Label)

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Principal Display Panel (1 mL Vial Carton)

This is a product page for Depo-Testosterone and Depo-Testosterone Cypionate, both injections for intramuscular use only. There are warnings about not using more than recommended and storing the product at controlled room temperature. The package contains one 10mL vial, and the imprint area reads "NO VARNISH" and "NO COPY."*

FDA Label Image

Depo 07

Depo®-Testosterone is an injection medication used for IM use only. Its active ingredient is Testosterone Cypionate. Each 10mL of medication is contained in a multiple-dose vial, and the concentration is 200mg/mL. The NDC number is 0009-0086-10 RXONLY.*

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Depo 08

This is a description for a medication called "Depo-Testosterone" in an injection form. The medication contains 200mg testosterone cypionate per 1ml. The medicine is for intramuscular use only and comes in a 10 ml vial. The vial should be warmed and shaken before use to redissolve any precipitates. The dosage and use information are available with the accompanying prescription information. It is distributed by Pharmacia & Upjohn, which is a division of Pfizer. The NDC code for the medication is 0009-0086-10. The text includes no non-English characters.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.