Metoclopramide Injection, Solution
Product Images NDC 0409-3414

6 FDA label images from Hospira, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Metoclopramide (NDC 0409-3414). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hospira, 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

Hospira Logo (Metoclopramide 01)

FDA Label Image

Structural Formula Metoclopramide Hydrochloride (Metoclopramide 02)

Structural Formula Metoclopramide Hydrochloride (Metoclopramide 02)
Chemical structure diagram of metoclopramide showing molecular groups, including chloro, amino, methoxy, diethylaminoethyl, hydrochloride, and water components. The molecular weight is indicated as 354.3.*
FDA Label Image

Hospira Logo (Metoclopramide 03)

FDA Label Image

Hospira Logo (Metoclopramide 04)

FDA Label Image

Principal Display Panel (2 mL Vial Label)

Principal Display Panel (2 mL Vial Label)
Label for Metoclopramide Injection, USP, 10 mg/2 mL (equivalent to 5 mg/mL), single-use vial for intravenous or intramuscular use. The label includes the NDC 0409-3414-18 and identifies Hospira, Inc. as the distributor located in Lake Forest, IL.*
FDA Label Image

Principal Display Panel (2 mL Vial Tray)

Principal Display Panel (2 mL Vial Tray)
Packaging label for Metoclopramide Injection, USP, 10 mg/2 mL (5 mg/mL) solution in single-use vials. The label indicates 25 vials per carton, manufactured by Hospira, Inc., with instructions for intramuscular and intravenous use. Storage and handling information is also included.*

* 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.