Verapamil Hydrochloride Injection, Solution
Product Images NDC 70069-273

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Verapamil Hydrochloride (NDC 70069-273). 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.

FDA Label Image

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FDA Label Image

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This is a prescription medication called Verapamil Hydrochloride intended for intravenous use only. It is manufactured by Somerset Therapeutics and comes in a single-dose 2mL vial. The medication contains 5mg/2mL and should be stored at 20°C to 25°C until ready to use. The expiration date and lot number are provided on the packaging. The text also advises users to discard any unused portion and protect the medication from light.*

FDA Label Image

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This is a description of a medication called Verapamil Hydrochloride Injection, USP. It is for intravenous use only and is manufactured by Somerset Therapeics. Each mL contains verapamil hydrochloride, sodium chloride, may contain hydrochloric acid and/or sodium hydroxide, and should be used only as directed. It is typically given as a slow intravenous injection over a period of time, and the usual dosage instructions can be found in the package insert. The medication should be stored at 2 to 25°C in a controlled room temperature and protected from light. The text also includes some other characters that do not provide any meaningful information.*

FDA Label Image

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Verapamil Hydrochloride Injection, USP is a medication used for pH adjustment and overprinting. It is available in a 2.5mg/mL concentration and is intended for intravenous use only. The dosage and usage instructions are available on the packaging insert. The medication should be stored at room temperature and protected from light when not in use. It is manufactured in India by Somerset Therapeutics LLC.*

FDA Label Image

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FDA Label Image

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Verapamil Hydrochloride Injection, USP is a medication that contains verapamil hydrochloride equivalent to 2.3 mg verapail and sodium chorde, used for intravenous use only. It is manufactured in India by Somerset Therapeutics and comes in 5 x 4 mL single-dose vials. The medication should be given as a slow intravenous injection over a period of at least two minutes. The usual dosage is mentioned in the package. It should be stored at a temperature of 20°C to 25°C and should be protected from light by keeping it in the carton ready for use. For more information, contact customer care at the provided phone number.*

FDA Label Image

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This appears to be a drug label that provides information about verapamil hydrochloride injection, which is meant for intravenous use only. It includes details about the manufacturing, composition, and dosage of the drug. Additionally, it provides instructions on how to use and store the medication.*

FDA Label Image

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FDA Label Image

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Verapamil Hydrochloride is an injection used for intravenous use only. It should be protected from light and comes in 5x2mL single-dose ampules. The product is produced by Somerset Therapeutics LLC and is formulated as Verapamil Hydrochloride Injection, USP, at a concentration of 2.5mg/mL. It is intended for intramuscular use only and should be stored at temperatures between 20°C to 25°C (68°F to 77°F). Each 1mL of the product contains 2.5gm of verapamil hydrochloride, 2.3mg of foquivalort verapamil, sodium chloride 85mg and may contain hydrochloric acid and/or sodium hydroxide for pH adjustment. The product is manufactured by Somerset Therapeutics, LLC in Hollywood, Fl. No additional information is available.*

* 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.