Risperidone Tablet, Film Coated
Product Images NDC 69367-371

7 FDA label images from Westminster Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Risperidone (NDC 69367-371). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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

Chemical Structure (Risperidone 01)

Chemical Structure (Risperidone 01)
Chemical structure of risperidone, the active ingredient in the risperidone oral film-coated tablet. The diagram shows the molecular layout including rings and functional groups characteristic of risperidone.*
FDA Label Image

0.25mg Tablets- Bottle Label-500's (Risperidone 02)

0.25mg Tablets- Bottle Label-500's (Risperidone 02)
Packaging label for Risperidone Tablets, USP 0.25 mg film-coated tablets, containing 500 tablets per container. The label includes dispensing instructions, storage conditions, and warnings to protect from light and moisture. Manufactured by Renata Limited in Bangladesh and distributed by Westminster Pharmaceuticals, LLC in Nashville, TN. Includes barcode and NDC 69367-368-05.*
FDA Label Image

0.5mg Tablets- Bottle Label-500's (Risperidone 03)

0.5mg Tablets- Bottle Label-500's (Risperidone 03)
Label for Risperidone Tablets, USP 0.5 mg by Westminster Pharmaceuticals, LLC. The film-coated oral tablets are packaged in a container of 500 tablets. The label includes storage instructions, manufacturer information (Renata Limited, Bangladesh), and distribution details (Westminster Pharmaceuticals, Nashville, TN). The label also features an NDC number 69367-369-05 and barcodes.*
FDA Label Image

1mg Tablets- Bottle Label-500's (Risperidone 04)

1mg Tablets- Bottle Label-500's (Risperidone 04)
Label for Risperidone Tablets, USP 1 mg oral film-coated tablets. The label states the product contains 500 tablets, is prescription only, and is distributed by Westminster Pharmaceuticals, LLC. It includes storage instructions, manufacturer details from Renata Limited in Bangladesh, and a barcode. The brand name 'risperiDONE' is prominently displayed with the strength in a purple capsule shape.*
FDA Label Image

2mg Tablets- Bottle Label-500's (Risperidone 05)

2mg Tablets- Bottle Label-500's (Risperidone 05)
Label for RisperiDONE Tablets, USP 2 mg oral film-coated tablets by Westminster Pharmaceuticals, LLC. The carton contains 500 tablets. The label includes dosage and storage instructions, manufacturer and distributor information, and the NDC 69367-371-05.*
FDA Label Image

3mg Tablets- Bottle Label-500's (Risperidone 06)

3mg Tablets- Bottle Label-500's (Risperidone 06)
Packaging label for Risperidone tablets, USP 3 mg film-coated oral tablets by Westminster Pharmaceuticals. The label states a package count of 500 tablets and includes storage instructions, manufacturer information (Renata PLC, Bangladesh), and distributor information (Westminster Pharmaceuticals, Nashville, TN). The NDC number 69367-372-05 is shown with a barcode.*
FDA Label Image

4mg Tablets- Bottle Label-500's (Risperidone 07)

4mg Tablets- Bottle Label-500's (Risperidone 07)
Label for Risperidone Tablets, USP 4 mg, film-coated oral tablets. The package contains 500 tablets. Labeler is Westminster Pharmaceuticals, LLC. The label includes storage instructions, dispensing notes, and manufacturer details in Bangladesh. The NDC number 69367-373-05 and barcode are also visible.*

* 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.