Dicyclomine Hydrochloride Capsule
Product Images NDC 24979-201

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dicyclomine Hydrochloride (NDC 24979-201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, 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

Image Description (Rld Structure)

Image Description (Rld Structure)
Chemical structure of Dicyclomine Hydrochloride showing its molecular formula including two cyclohexane rings linked by an ester and amine group, with a molecular weight of 345.95.*
FDA Label Image

100-count (Dicyclomine Hydrochloride Capsules Usp Dicyclomine 2)

100-count (Dicyclomine Hydrochloride Capsules Usp Dicyclomine  2)
Label for Dicyclomine Hydrochloride Capsules, USP 10 mg, showing the prescription drug in capsule form. The label states the dosage strength as 10 mg, contains 100 capsules, and is manufactured by TWi Pharmaceuticals, with addresses in Paramus, NJ, and Taoyuan City, Taiwan. The NDC number 24979-201-01 and barcode are visible, along with storage instructions and a caution to keep out of reach of children.*
FDA Label Image

1000-count (Dicyclomine Hydrochloride Capsules Usp Dicyclomine 3)

1000-count (Dicyclomine Hydrochloride Capsules Usp Dicyclomine  3)
Label for Dicyclomine Hydrochloride Capsules, USP, 10 mg strength, in a bottle containing 1000 capsules. The label includes dosing and storage instructions, manufacturer information (TWi Pharmaceuticals USA and Taiwan), and the product NDC 24979-201-03. It is marked Rx only.*
FDA Label Image

Image Description (Logo 2)

* 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.