Clonidine Injection, Solution
Product Images NDC 39822-2000

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Clonidine (NDC 39822-2000). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xgen Pharmaceuticals Djb, 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

Clon Cs100 05

This is a product description for Clonidine Hydrochloride Injection, which is used as a sedative, analgesic and anesthetic adjuvant. The injection comes in a 10mLsingle-dose vial, and is for epidural injection. The dosage should be followed as per the package insert. The product is manufactured in the USA.*

FDA Label Image

Clon Vl100 03

This is a medication with the National Drug Code (NDC) 39822-2000-1, available in a single-dose vial of 10 milliliters. It contains Clonidine Hydrochloride and is administered via injection. The concentration of Clonidine Hydrochloride in each 10ml dosage is 1000 micrograms.*

FDA Label Image

Clonidine 5000 Vial

This is a label for Clonidine Hydrochloride injection with a strength of 5000 mcg/10 mL (500 mcg/mL). It is packaged in a 10 ml single-dose vial bearing a lot number but with no expiry date mentioned.*

FDA Label Image

Carton 5000 Clonidine

This appears to be a product label with information regarding a medication called Clonidine Hydrochloride. It includes details such as the manufacturer's location, storage instructions, dosage information, and packaging. The medication is available in a single-dose vial and is non-pyrogenic.*

FDA Label Image

Clonidine-structure (Clonidine HCl Injection 1)

* 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.