Cevimeline Capsule
Product Images NDC 63304-479

2 FDA label images from Sun Pharmaceutical Industries, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Cevimeline (NDC 63304-479). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

The Structural Formula For Cevimeline Has A Molecular Weight Of 244.79. It Is A White To Off White Crystalline Powder With A Melting Point Range Of 201 To 203oc. It Is Freely Soluble In Alcohol And Chloroform, Very Soluble In Water, And Virtually Insoluble In Ether. The Ph Of A 1% Solution Ranges From 4.6 To 5.6. Inactive Ingredients Include Lactose Monohydrate, Hydroxypropyl Cellulose, And Magnesium Stearate. (Cevimeline 01)

The Structural Formula For Cevimeline Has A Molecular Weight Of 244.79. It Is A White To Off White Crystalline Powder With A Melting Point Range Of 201 To 203oc. It Is Freely Soluble In Alcohol And Chloroform, Very Soluble In Water, And Virtually Insoluble In Ether. The Ph Of A 1% Solution Ranges From 4.6 To 5.6. Inactive Ingredients Include Lactose Monohydrate, Hydroxypropyl Cellulose, And Magnesium Stearate. (Cevimeline 01)
Chemical structure of Cevimeline hydrochloride monohydrate, showing the molecular arrangement including a bicyclic amine, a sulfur-containing ring, and a methyl group.*
FDA Label Image

Principal Display Panel Ndc 63304-479-01 Cevimeline Hydrochloride Capsules 30 mg 100 Capsules Rx Only (Cevimeline 02)

Principal Display Panel Ndc 63304-479-01 Cevimeline Hydrochloride Capsules 30 mg 100 Capsules Rx Only (Cevimeline 02)
Label of Cevimeline Hydrochloride capsules, 30 mg, manufactured by Sun Pharmaceutical Industries, Inc. The label shows the NDC 63304-479-01 and indicates the package contains 100 capsules. It includes storage instructions and a barcode on the left side.*

* 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.