Prazosin Hydrochloride Capsule
Product Images NDC 71610-694

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 Prazosin Hydrochloride (NDC 71610-694). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Bottle Label 1 mg (71610 0693 30)

Bottle Label 1 mg (71610 0693 30)
Prazosin Hydrochloride 1 mg capsule label showing the product name, strength, and quantity of 30 capsules. The label includes storage instructions, manufacturer details as Granules Pharmaceuticals, Inc. (Chantilly, VA), and repackager Aphena Pharma Solutions - Tennessee, LLC (Cookeville, TN). It features a barcode, NDC code 7610-0693-30, and RX only designation.*
FDA Label Image

Bottle Label 2 mg (71610 0694 30)

Bottle Label 2 mg (71610 0694 30)
Label for Prazosin Hydrochloride 2 mg capsules, containing 30 capsules. The label includes storage instructions to keep between 20-25 degrees Celsius and to dispense in a tight, light-resistant container. Manufactured by Granules Pharmaceuticals, Inc., Chantilly, VA. Packaged by Aphena Pharma Solutions - Tennessee, LLC. The label shows the NDC number 71610-0694-30 and includes lot number, expiration date, and barcode.*
FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of prazosin hydrochloride showing its molecular formula C19H21N5O4·HCl with labeled rings and functional groups.*

* 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.