Ropivacaine Hydrochloride Injection, Solution
Product Images NDC 25021-652

3 FDA label images from Sagent Pharmaceuticals · 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 Ropivacaine Hydrochloride (NDC 25021-652). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent 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

Figure (Rop02 0010 01)

Figure (Rop02 0010 01)
Chemical structure diagram of Ropivacaine Hydrochloride, showing its molecular composition including a piperidine ring, aromatic ring, and associated hydrochloride and water molecules.*
FDA Label Image

Package Label – Principal Display Panel – Bag Label (Rop02 0010 02)

Package Label – Principal Display Panel – Bag Label (Rop02 0010 02)
Label for Ropivacaine HCl Injection, USP 0.2% (2 mg/mL) in a 100 mL bag, containing 200 mg total active ingredient. The label states it is for infiltration, nerve block, and epidural administration only, not for intravenous use. Manufacturer is Sagent Pharmaceuticals, with additional formulation and storage information included.*
FDA Label Image

Package Label – Principal Display Panel – Bag Label (Rop02 0010 03)

Package Label – Principal Display Panel – Bag Label (Rop02 0010 03)
Label for Ropivacaine HCl Injection, USP, 5 mg/mL (0.5%) in a 100 mL bag. The label specifies the product is for infiltration, nerve block, and epidural administration only, and is not for intravenous use. It is a single-dose container made by Sagent Pharmaceuticals, manufactured in Switzerland. The label includes storage and sterile handling instructions.*

* 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.