Metoclopramide Injection, Solution
Product Images NDC 71872-7076

6 FDA label images from Medical Purchasing Solutions, Llc · 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 71872-7076). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

Pdp (7076)

Pdp (7076)
Metoclopramide Injection, USP 10 mg per 2 mL (5 mg/mL) single-use vial label. It includes dosing information, storage instructions, and manufacturer details. The label specifies intramuscular and intravenous administration and notes the vial is preservative-free and sterile. Manufactured by Hospira, inc. and repackaged by Medical Purchasing Solutions, LLC.*
FDA Label Image

Hospira Logo (Metoclopramide 01)

FDA Label Image

Structural Formula Metoclopramide Hydrochloride (Metoclopramide 02)

Structural Formula Metoclopramide Hydrochloride (Metoclopramide 02)
Chemical structure of metoclopramide hydrochloride monohydrate showing the molecular formula with chlorine, amine, methoxy groups, and molecular weight of 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 per 2 mL (5 mg/mL) in a 2 mL single-use vial. The label indicates the injection is for intravenous (I.V.) or intramuscular (I.M.) use and is prescription only. Manufactured by Hospira, Inc., Lake Forest, IL, with NDC 0409-3414-18.*

* 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.