Risperidone
Product Images NDC 64725-0321

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 Risperidone (NDC 64725-0321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Tya Pharmaceuticals, 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 Image (64725 0319)

Label Image (64725 0319)
This is a description of a medication called Risperidone 2HG Tablet, which comes in a package of 30 tablets. The medicine is intended for prescription-only use and has a unique code of 51991-319-08. The label shows the lot number as "000" and the expiry date is "XX-XX-XX". The manufacturer of the drug is Ajanta Pharma. However, the medication has been repackaged by TY.A. Pharmaceuticals at their address, 2030 Caescent Dr., Tallahassee, FL 32301. They can be contacted at (850) 385-0228 for more information. There is no information available on the dosage of the medicine, hence the package insert has to be referred to.*
FDA Label Image

Label Image (64725 0321)

Label Image (64725 0321)
This is a medication called Risperidone, which comes in the form of a 4mg tablet. This medicine is available only with a prescription and requires authorization (code S0CTCD). The label includes a lot number (20000) and an expiration date that is not legible. It was manufactured by Ajanta Pharma but repackaged by T.Y.A Pharmaceuticals located in Tallahassee, FL. For dosage instructions, see the package insert.*
FDA Label Image

Approximate (Risperidone Equal)

FDA Label Image

Structure (Risperidone Str)

* 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.