Sterile Diluent For Treprostinil Injection, Solution
Product Images NDC 43598-126

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Sterile Diluent For Treprostinil (NDC 43598-126). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories 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

100mgcarton (100mgcarton)

100mgcarton (100mgcarton)
The unfolded carton label for Treprostinil Injection, 100 mg/20 mL (5 mg/mL), a solution for injection for subcutaneous or intravenous infusion only. The label indicates a 20 mL multiple-dose vial, Rx only, distributed by Dr. Reddy's Laboratories Inc. Dosage and storage instructions are partially visible, along with the barcode and manufacturer details indicating it is made in India.*
FDA Label Image

200mgcarton (200mgcarton)

200mgcarton (200mgcarton)
Packaging label for Treprostinil Injection 200 mg/20 mL (10 mg/mL) multiple-dose vial. The label states it is for subcutaneous or intravenous infusion only, contains 20 mL, and is labeled Rx only. The labeler is Dr. Reddy's Laboratories Inc., with storage instructions and ingredient details included.*
FDA Label Image

20mgcarton (20mgcarton)

20mgcarton (20mgcarton)
Packaging label for Treprostinil Injection 20 mg/20 mL (1 mg/mL) solution for injection by Dr. Reddy's Laboratories Inc. The 20 mL multiple-dose vial is intended for subcutaneous or intravenous infusion only. The label includes storage instructions, ingredients, NDC 43598-649-11, and barcode.*
FDA Label Image

50mgcarton (50mgcarton)

50mgcarton (50mgcarton)
Packaging label for Treprostinil Injection 50 mg/20 mL (2.5 mg/mL) solution for injection. The label specifies use for subcutaneous or intravenous infusion only and indicates a 20 mL multiple-dose vial. It includes manufacturer information for Dr. Reddy's Laboratories Inc. and lists excipients such as sodium citrate dihydrate and sodium chloride. The label contains barcodes, storage instructions, and safety notes to keep out of reach of children.*
FDA Label Image

Diluent (Diluent)

Diluent (Diluent)
Label for Sterile Diluent for Treprostinil Injection, 50 mL vial. The label states it contains drug diluent for use only with intravenous infusion of treprostinil injection. Labeler is Dr. Reddy's Laboratories, Inc., Princeton, NJ, with product made in India. Storage and ingredient details are provided.*
FDA Label Image

Diluentcarton (Diluentcarton)

Diluentcarton (Diluentcarton)
Packaging label for Treprostinil Sterile Diluent Injection, 1 x 50 mL vial by Dr. Reddy's Laboratories Inc. The label includes storage instructions, ingredient information for each vial, and usage notes specifying it is for intravenous infusion of treprostinil. The label also displays barcodes, the NDC 43598-126-11, and distributor details.*
FDA Label Image

Figure 1 (Figure1)

Figure 1 (Figure1)
A Kaplan-Meier survival curve showing the percentage of subjects without a clinical deterioration event over days on study. Two groups are compared: Treprostinil treatment (solid line) and placebo (dashed line). The graph indicates a statistically significant difference (p=0.000228) favoring Treprostinil in preventing clinical deterioration over approximately 60 days.*
FDA Label Image

Chemical Structure (Struture)

Chemical Structure (Struture)
Chemical structure of Treprostinil, a human prescription drug injection solution by Dr.Reddy's Laboratories Inc. The diagram shows the molecular composition with labeled hydroxyl groups and carboxyl group, including a hydration component (H2O).*

* 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.