Prazosin Hydrochloride Capsule
Product Images NDC 0093-4068

4 FDA label images from Teva Pharmaceuticals Usa, Inc. · 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 0093-4068). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals Usa, 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

Prazosin Hydrochloride Capsule 071745 1

Prazosin Hydrochloride Capsule 071745 1
Chemical structure diagram of Prazosin Hydrochloride showing detailed molecular bonds and groups, including methoxy and amine groups, and the hydrochloride component.*
FDA Label Image

Prazosin Hydrochloride Capsule 071745 2

Prazosin Hydrochloride Capsule 071745 2
Label for Prazosin Hydrochloride Capsules USP 1 mg by Teva Pharmaceuticals USA, Inc. The label indicates 100 capsules per bottle for oral use. It includes storage instructions, dosage notes, and safety warnings, alongside a barcode and NDC 0093-4067-01.*
FDA Label Image

Prazosin Hydrochloride Capsule 071745 3

Prazosin Hydrochloride Capsule 071745 3
Label for Prazosin Hydrochloride Capsules USP 2 mg, an oral prescription drug by Teva Pharmaceuticals USA, Inc. The label indicates a package containing 100 capsules. Storage instructions and warnings to protect from light and moisture, as well as child safety precautions, are included. The label displays the NDC 0093-4068-01 and barcode.*
FDA Label Image

Prazosin Hydrochloride Capsule 071745 4

Prazosin Hydrochloride Capsule 071745 4
Label for Prazosin Hydrochloride Capsules USP 5 mg by Teva Pharmaceuticals USA, Inc. The label shows it contains 100 capsules, with storage instructions and warnings about light and moisture. The label includes the NDC 0093-4069-01 and states "Rx only."*

* 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.