Dicyclomine Hydrochloride Tablet
Product Images NDC 73473-902
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dicyclomine Hydrochloride (NDC 73473-902). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Solaris Pharma Corporation, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
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This text provides important details about Dicyclomine Hydrochloride Tablets, USP. Each tablet contains 20 mg of Dicyclomine hydrochloride. The usual dosage information can be found in the package outsert. It is recommended to dispense these tablets in a tight, light-resistant container with a child-resistant closure. The storage instructions advise keeping the package between 20 to 25°C (68° to 77°F) and protecting it from direct sunlight, light, and moisture to prevent fading. Additionally, this medication should be kept out of reach of children. The tablets are manufactured for Solaris Pharma Corporation located in Somerset, NJ.*
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This text provides information about Dicyclomine Hydrochloride Tablets, USP. Each tablet contains 20 mg of Dicyclomine hydrochloride. The usual dosage should be checked on the package outsert for prescribing information. The medication should be dispensed in a child-resistant container and stored at 20°C to 25°C (68°F to 77°F) to prevent fading, avoiding direct sunlight exposure, and protecting from light and moisture. The product is manufactured by Solaris Pharma Corporation for Somerset, NJ 08873, with an item code #40339 and the revision date of 04/2025.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.