Diluent Injection
Product Images NDC 0781-6021

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Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diluent (NDC 0781-6021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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

Treprostinil Chemical Structure (Treprostinil Image 01)

FDA Label Image

Figure 1 (Treprostinil Image 02)

FDA Label Image

20mg-carton (Treprostinil Image 03)

20mg-carton (Treprostinil Image 03)
This is a medication with the brand name "Treprostini". It comes in a 20mg/20mL dosage and is injected. It is contained in a multi-dose vial and is diluted for subcutaneous or intravenous infusion. The usual dosage should be seen on the package insert. It is important to store the medication at 20°C to 25°C and keep it out of reach of children. The medication is manufactured by Sandoz.*
FDA Label Image

50mg-carton (Treprostinil Image 04)

50mg-carton (Treprostinil Image 04)
This is a description of Treprostinil, which is an injection medication used for intravenous infusion or subcutaneous use, and comes in a 20 mL multi-dose vial. Each milliliter contains 2.5mg/ml of Treprostinil with phosphate-buffered saline and metacresol as additives, which are required to adjust the pH level of the drug. The usual dosage of the medication can be found in the package insert. This medication is stored at room temperature, away from children. The text also contains NDC and Rx-only codes, as well as the manufacturer's contact information.*
FDA Label Image

100mg-carton (Treprostinil Image 05)

100mg-carton (Treprostinil Image 05)
This text describes a medication called Treprostinil available in a 20 mL Mult-Dose Vial manufactured by Sandoz. Each mL contains 5 mg of Treprostinil along with other ingredients such as sodium citrate and metacresol. It is stated that hydrochloric acid and sodium hydroxide may have been added to adjust the pH of the medication. The medication is to be used for subcutaneous or intravenous infusion only, and the usual dosage should be determined according to the package insert. The medication needs to be diluted prior to use and should be stored at a temperature of 20° to 25°C. The National Drug Code (NDC) for this product is 0781-3427-80.*
FDA Label Image

200mg-carton (Treprostinil Image 06)

200mg-carton (Treprostinil Image 06)
Treprostinil Injection is a medication produced by Sandoz, and the NDC code is 0751-3430-80. It comes in a 20 mL multi-dose vial, and each mL of this medication contains ten milligrams of treprostinil. This treatment requires either subcutaneous or intravenous infusion, and its concentration is 10 milligrams per milliliter. This medication should be kept at room temperature and out of reach of children. The package insert provides detailed information on the standard dosage.*
FDA Label Image

Diluent-carton (Treprostinil Image 07)

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