Diphenoxylate Hydrochloride And Atropine Sulfate Tablet
Product Images NDC 71335-1693

3 FDA label images from Bryant Ranch Prepack · 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 Diphenoxylate Hydrochloride And Atropine Sulfate (NDC 71335-1693). 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

Chemicalstructureatropine (Chemstructure 01)

Chemicalstructureatropine (Chemstructure 01)
Chemical structure diagram showing two molecules of atropine sulfate monohydrate. The structure includes a bicyclic tropane ring with a methyl group on the nitrogen, an ester linkage to a phenyl group, and associated sulfate and water molecules.*
FDA Label Image

Chemicalstructurediphen (Chemstructure)

Chemicalstructurediphen (Chemstructure)
Chemical structure diagram of diphenoxylate hydrochloride, the active ingredient in Diphenoxylate Hydrochloride and Atropine Sulfate tablets by Bryant Ranch Prepack.*
FDA Label Image

Label Image (Lbl713351693)

Label Image (Lbl713351693)
Label for Diphenoxylate Hydrochloride and Atropine Sulfate tablets, strength 2.5 mg/0.025 mg, oral dosage form. The label indicates it is packaged by Bryant Ranch Prepack, Burbank, CA, with a compare to Lomotil (CV) Tablet by Leading Pharma, LLC. The package contains 20 tablets, with a space for expiration date and a highlighted NDC number 71335-1693-1. Additional label information includes storage instructions, drug safety warnings, lot number, and a barcode.*

* 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.