Dexamethasone Sodium Phosphate Injection
Product Images NDC 70069-021

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Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dexamethasone Sodium Phosphate (NDC 70069-021). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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.

Product Images & Figures Index

FDA Label Image

42109b8e 9bb6 403c A82d B64cf453d7e5 01

42109b8e 9bb6 403c A82d B64cf453d7e5 01
This is a chemical formula for a compound consisting of sodium phosphate (CH, OPO(ONa)) and calcium fluoride (Ca,H2eFNa). The molecular weight of the compound is 516.41 grams per mole.*
FDA Label Image

42109b8e 9bb6 403c A82d B64cf453d7e5 02

42109b8e 9bb6 403c A82d B64cf453d7e5 02
This is a description of a medication called Dexamethasone Phosphate Injection, which is manufactured for Somerset Therapeutics, LLC in Hollywood, FL. Each single-dose vial contains 10mg of Dexamethasone Phosphate and Sodium Phosphate. It is for intramuscular or intravenous use only and should be protected from light. The medication is preservative-free and any unused portion must be discarded. The code number and sterile information are also provided. The text also includes a note about a "No Varnish Area" that measures 15x4.5mm, although it is unclear what this refers to exactly.*
FDA Label Image

42109b8e 9bb6 403c A82d B64cf453d7e5 03

42109b8e 9bb6 403c A82d B64cf453d7e5 03
This is a description for a drug called Dexamethasone Sodium Phosphate Injection, USP that is manufactured in India by Somerset Therapeutics, LLC. The active ingredient is Dexamethasone Phosphate and each mL contains 10 mg of it. The drug is used for Intramuscular or Intravenous use only and is Preservative-free and sterile. The vial stopper closure is not made with natural rubber latex. The usual dosage and storage instructions are mentioned in the package insert. The drug comes in a container of 25 x 1 L Single Dose Vials, and unused portions should be discarded. The information about the manufacturer and customer care is provided. The code no. KR/DRUGSIKTK/28/28997 and the reference no. ST-DEX21/C25/02 are mentioned on the package. However, the text also includes some unrelated characters and digits that seem to be a result of errors.*

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