Ropivacaine Hydrochloride Injection
Product Images NDC 70121-1734

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Ropivacaine Hydrochloride (NDC 70121-1734). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal 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

1 (Ropivacaine Hydrochloride Injection 1)

Chemical structure diagram of Ropivacaine Hydrochloride showing its molecular components including a benzene ring, amide group, piperidine ring, and associated hydrochloride and water molecules.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 2)

Label section showing manufacturing and distribution information for Ropivacaine Hydrochloride injection. Manufactured by Amneal Injectables Private Limited in Mehsana, India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, New Jersey.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 3)

A red label panel indicating usage instructions for Ropivacaine Hydrochloride injection. The label states "FOR INFILTRATION, NERVE BLOCK AND EPIDURAL USE ONLY" in black text. A peel-off tab on the side repeats the usage warning in vertical text.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 4)

Label for Ropivacaine Hydrochloride Injection, USP 0.2% (2 mg/mL) in a 100 mL single-dose infusion bag. The injection is for infiltration, nerve block, and epidural administration. It is preservative free, sterile, and distributed by Amneal Pharmaceuticals LLC. The label includes dosage information, storage conditions, and manufacturing details from India.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 5)

Label for Ropivacaine Hydrochloride Injection, USP 0.2% (2 mg/mL) in a 100 mL single-dose infusion bag. The label specifies use for infiltration, nerve block, and epidural administration, and notes the product is sterile and preservative-free. It includes manufacturer information for Amneal Injectables Private Limited and distributor details for Amneal Pharmaceuticals LLC.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 6)

Label for Ropivacaine Hydrochloride Injection, USP, 0.2% strength (2 mg/mL; 200 mg per 100 mL), in a 100 mL bag, packaged 24 units. Indicated for infiltration, nerve block, and epidural administration. Manufactured by Amneal Injectables Private Limited, India, and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Single-dose, preservative-free, sterile injection.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 7)

Ropivacaine Hydrochloride Injection, USP 5 mg/mL (0.5%) in a 100 mL single-dose vial label by Amneal Pharmaceuticals LLC. The label specifies use for infiltration, nerve block, and epidural administration. It lists active and inactive ingredients, directions to discard unused portions, and storage conditions.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 8)

Ropivacaine Hydrochloride Injection, USP label for a 100 mL single-dose vial containing 5 mg/mL (0.5%) solution. The label indicates use for infiltration, nerve block, and epidural administration. Manufactured by Amneal Injectables Private Limited (India) and distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Includes storage instructions and composition details.*

FDA Label Image

1 (Ropivacaine Hydrochloride Injection 9)

Label for Ropivacaine Hydrochloride Injection USP, 5 mg/mL (0.5%), presented as 500 mg per 100 mL in 10 x 100 mL bags. Intended for infiltration, nerve block, and epidural administration. Manufactured by Amneal Injectables Private Limited and distributed by Amneal Pharmaceuticals LLC.*

* 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.