Lacosamide Injection, Solution
Product Images NDC 70069-471
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This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Lacosamide (NDC 70069-471). 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
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This is a product label for Lacosamide Injection, USP with a concentration of 200 mg/20 mL. It is indicated for intravenous use only and should be discarded if unused. The usual dosage information can be found in the package insert. The storage temperature ranges from 20°C to 25°C, with excursions permitted between 15°C to 30°C. It should not be frozen. The product is manufactured for Somerset Therapeutics, LLC in Somerset, NJ, and made in India. The label also includes a code number for identification purposes.*
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This is a description of a medication, Lacosamide, in the form of a 20 mL solution for infusion. The solution contains 200 mg of Lacosamide, USP per single-dose vial. It is manufactured by Somerset Therapeutics, LLC in Somerset, NJ. The inactive ingredients include sodium chloride, hydrochloric acid, and water for injection. The usual dosage information can be found in the package insert. The medication should be stored at 20°C to 25°C, with excursions permitted between 15°C to 30°C. It should not be frozen and is for intravenous use only. A Medication Guide should be dispensed to each patient, and it is advised to keep the medication out of reach of children.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.