Diphenoxylate Hydrochloride And Atropine Sulfate
Product Images NDC 67296-1675

3 FDA label images from Redpharm Drug, Inc. · 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 67296-1675). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, Inc., 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

Label (Diphenoxylate 1675)

Label (Diphenoxylate 1675)
Label of Diphenoxylate Hydrochloride and Atropine Sulfate tablets, strength 2.5 mg/0.025 mg, containing 15 tablets. The label shows it is Rx only with lot number 27476BX1 and expiration 07/20. Manufactured by Lannett Company Inc., Philadelphia, PA, and distributed by RedPharm Drug, Inc., Eden Prairie, MN. Storage instructions and barcode are also visible.*
FDA Label Image

Dip Structural Formula (Diphenoxylate Hydrochloride And Atropine Sulfate T 1)

Dip Structural Formula (Diphenoxylate Hydrochloride And Atropine Sulfate T 1)
Chemical structure of diphenoxylate hydrochloride shown as a molecular diagram with various chemical groups and bonds.*
FDA Label Image

Atropine Sulfate Structural Formula (Diphenoxylate Hydrochloride And Atropine Sulfate T 2)

Atropine Sulfate Structural Formula (Diphenoxylate Hydrochloride And Atropine Sulfate T 2)
Chemical structure of the active ingredients in DIPHENOXYLATE HYDROCHLORIDE AND ATROPINE SULFATE from RedPharm Drug, Inc. The structure shows a bicyclic compound with substituents including methyl, hydroxyl, acetoxy, and phenyl groups, along with associated water and sulfuric acid molecules as hydrates.*

* 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.