Dicyclomine Hydrochloride Tablet
Product Images NDC 71335-0425

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Dicyclomine Hydrochloride (NDC 71335-0425). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Dicyclomine-hcl-molec-struc (Dicyclomine Hydrochloride Tablets Usp Dicyclomine 1)

This appears to be a chemical formula or notation. The molecular weight is given as 345.95. However, it is not clear what the specific compound or molecule being referred to is.*

FDA Label Image

Label Image (Lbl713350425)

This is a description of a medication named Dicyclomine Hydrochloride Tablets. Each tablet contains 20 mg of USP Dicyclomine Hydrochloride. The tablets are intended for prescription use only, and come in a bottle with 30 tablets. It is important to store the tablets at a temperature of 20° to 25° C (68° to 77° F) and there is some leeway to store them at 15° to 30° C (59° to 86° F) as well. This medication may cause dizziness or drowsiness. The information also includes an NDC (National Drug Code) number of 63629-1299-01.*

FDA Label Image

Lbl7133504252

This is a medication information sheet for Dicyclomine, an anti-spasmodic medication used to treat irritable bowel syndrome (IBS). It is manufactured by Lannett Company, Inc. and is distributed in blue, round pills with the code LAN; 1282, containing 20mg of HCL. The medication may cause dizziness or drowsiness and should be stored at room temperature between 20°-25°C (68°-77°F). It is also marked with an expiration date of MM/YY and NDC 7133504251 01299301523487.*

* 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.