Nouress
Product Images NDC 76014-006

3 FDA label images from Avadel Legacy Pharmaceuticals, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Nouress (NDC 76014-006). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avadel Legacy 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 (Nouress 01)

Chemical Structure (Nouress 01)
Chemical structure of the active ingredient showing an amino acid with a thiol group, carboxyl group, amine group, and associated hydrochloride (HCl) and water (H2O) molecules, likely representing the hydrochloride hydrate form of the compound in Nouress by Avadel Legacy Pharmaceuticals, LLC.*
FDA Label Image

Vial Label (Nouress 02)

Vial Label (Nouress 02)
The label for Nouress (cysteine hydrochloride injection), USP shows a strength of 500 mg/10 mL (50 mg/mL) in a 10 mL single-dose vial. It indicates the product is sterile and for intravenous infusion only, requiring dilution. The label includes dosage formulation details, storage instructions, lot number, expiration date, and manufacturer Avadel Legacy Pharmaceuticals, LLC.*
FDA Label Image

Carton Label (Nouress 03)

Carton Label (Nouress 03)
Packaging label for Nouress (cysteine hydrochloride injection), USP, 500 mg/10 mL (50 mg/mL), manufactured by Avadel Legacy Pharmaceuticals, LLC. The label indicates it is a sterile, single-dose vial product supplied as 5 x 10 mL vials, intended for intravenous infusion only, and must be diluted before use.*

* 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.