Product Images Remodulin

View Photos of Packaging, Labels & Appearance

Product Label Images

The following 8 images provide visual information about the product associated with Remodulin NDC 66302-105 by United Therapeutics Corporation, such as packaging, labeling, and the appearance of the drug itself. This resource could be helpful for medical professionals, pharmacists, and patients seeking to verify medication information and ensure they have the correct product.

Chemical Structure - remodulin 01

Chemical Structure - remodulin 01

Figure 1 - remodulin 02

Figure 1 - remodulin 02

Principal Display Panel - 1 mg/mL Vial Carton - remodulin 03

Principal Display Panel - 1 mg/mL Vial Carton - remodulin 03

PRINCIPAL DISPLAY PANEL - 2.5 mg/mL Vial Carton - remodulin 04

PRINCIPAL DISPLAY PANEL - 2.5 mg/mL Vial Carton - remodulin 04

This text contains information about a medication called REMODULIN (treprostinil) Injection that comes in a 20 mL multidose vial. The medication is intended for subcutaneous or intravenous infusion only and must be diluted prior to intravenous infusion. Each mL of the medication contains 2.5 mg treprostinil, along with other ingredients such as sodium citrate, sodium chloride, and metacresol. The package insert provides information about dosage and administration. The medication is manufactured by United Therapeutics Corp. in RTP, NC, USA. Storage instructions indicate that the medication should be kept at 25°C with excursions permitted to 2:30°C.*

PRINCIPAL DISPLAY PANEL - 5 mg/mL Vial Carton - remodulin 05

PRINCIPAL DISPLAY PANEL - 5 mg/mL Vial Carton - remodulin 05

REMODULIN is a medication given through subcutaneous or intravenous infusion for the treatment of pulmonary arterial hypertension. It is available in a 20 ml multidose vial containing 100 mg/20 mL of treprostinil injection with added Hydrochloric acid and Sodium hydrard to adjust pH level. The medication is being manufactured by United Therapeutics Corp. Note: technology has inaccurately recognized certain words/characters in the original text, and as a result, some of the information may not be entirely accurate.*

PRINCIPAL DISPLAY PANEL - 10 mg/mL Vial Carton - remodulin 06

PRINCIPAL DISPLAY PANEL - 10 mg/mL Vial Carton - remodulin 06

PRINCIPAL DISPLAY PANEL - 50mL Vial Carton - remodulin 07

PRINCIPAL DISPLAY PANEL - 50mL Vial Carton - remodulin 07

Remodulin is a medication that is administered either through subcutaneous or intravenous infusion. This medication contains treprostinil, which must be diluted before use. Remodulin comes in a 20 mL multidose vial containing 400 mg/20 mL (20 mg/mL) of the medication. The dosage and administration instructions are available in the package insert. The medication must be kept out of reach of children. The text also includes information about the composition of the medication and the storage conditions.*

remodulin 08

remodulin 08

This text provides information on a sterile diluent that is meant to be used only for intravenous infusion with REMODULIN (treprostinil) injection. The diluent contains alycine, sodium chloride, sodium hydroxide, and water for injection. It also provides storage instructions and a product code.*

* The product label images have been analyzed using a combination of traditional computing and machine learning techniques. It should be noted that the descriptions provided may not be entirely accurate as they are experimental in nature. Use the information in this page at your own discretion and risk.