Product Images Rotop - Dmsa
View Photos of Packaging, Labels & Appearance
Product Label Images
The following 5 images provide visual information about the product associated with Rotop - Dmsa NDC 71647-001 by Rotop Pharmaka Gmbh, 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.
rotop dmsa 01
rotop dmsa 02
This is a medication indicated for use in infants, children, and adults. It is meant for intravenous use and must be reconstituted and labeled before administration. The package contains 1.74 mg of powder for injection. Lot number and expiration date are not provided.*
rotop dmsa 03
ROTOP - DMSA 1.0 mg is a radiopharmaceutical preparation kit containing Succimer, which can be used in infants, children, and adults. Each kit contains 5 vials, and each vial contains 1.74 mg of powder to be used to make an injection solution. The active substance, Succimer, is present in each vial at a concentration of 1.0 mg. The excipients present in the preparation include stannous chloride dihydrate, ascorbic acid, sodium hydroxide, hydrochloric acid, and nitrogen. The solution is for intravenous use after reconstitution and labeling. It is recommended to store the original package in the fridge at a temperature range of 2 - 8 °C to protect it from light. The product should be kept out of the sight and reach of children. The product is a pharmacy-only medicine bearing the MA Number 3003663.00.00 and manufactured by ROTOP Pharmaka GmbH, located at Bautzner LandstraBe 400, 01328 Dresden, Germany.*
rotop dmsa 04
This is a product intended for intravenous use in infants, children, and adults. It comes in the form of a powder that needs to be reconstituted and labeled before use. The lot and expiration date are not available.*
rotop dmsa 05
ROTOP - DMSA 1.0 mg is a radiopharmaceutical preparation kit for use in infants, children and adults. Each of the 5 vials contains 1.74 mg powder for injection, comprising of an active substance of 1.0 mg succimer, and excipients such as stannous chloride dihydrate, ascorbic acid, sodium hydroxide, hydrochioric acid, and nitrogen. The reconstituted product is intended for intravenous use after labeling. It should be stored in the original package in a refrigerator at 2 - 8 °C, protected from light, and kept out of reach of children. This product is a pharmacy-only medicine and is manufactured by ROTOP Pharmaka GmbH in Germany.*
* 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.
