Metoclopramide Injection, Solution
Product Images NDC 76045-213

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Metoclopramide (NDC 76045-213). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

Met0p 0006 01

Chemical structure diagram of Metoclopramide Hydrochloride monohydrate, illustrating the molecular composition including a chlorinated aromatic ring, amine and methoxy groups, and ethyl side chains, consistent with the active ingredient in the Metoclopramide injection solution.*

FDA Label Image

Met0p 0006 02

An illustration of a Metoclopramide injection syringe, showing a 10 mg/2mL dosage form. The diagram labels parts of the syringe including the removable syringe tip cap, the plastic wrap which should not be removed, and the external collar which also should not be removed. It depicts the syringe as used for intramuscular or intravenous administration.*

FDA Label Image

Met0p 0006 03

An instructional line drawing showing two hands preparing a syringe with a vial, illustrating the process of drawing medication from the vial into the syringe, relevant for Metoclopramide Hydrochloride injection.*

FDA Label Image

Met0p 0006 04

An instructional illustration showing the steps to prepare an injection vial. The image depicts a hand twisting off the cap of a vial, demonstrating proper vial opening technique for an injection drug product.*

FDA Label Image

Met0p 0006 05

FDA Label Image

Met0p 0006 06

Metoclopramide Injection, USP 10 mg/2 mL (5 mg/mL) vial carton label from Fresenius Kabi USA, LLC. The packaging indicates 24 prefilled single-use syringes for intravenous or intramuscular injection, with instructions to discard unused portion and a note that a medication guide is attached to the professional package insert.*

FDA Label Image

Met0p 0006 07

Metoclopramide Injection, USP 10 mg/2 mL (5 mg/mL) single-use prefilled syringe label. Intended for intravenous or intramuscular use, labeled for prescription only by Fresenius Kabi USA, LLC. Storage instructions and barcode present, along with placeholders for expiration date and lot number.*

FDA Label Image

Met0p 0006 08

Label for Metoclopramide 10 mg/2 mL Injection, USP, by Fresenius Kabi USA, LLC. The label indicates the product is for IV or IM use, single-use vial with volume graduations up to 2 mL. It states the concentration as 5 mg/mL and includes a barcode and the note Rx only.*

FDA Label Image

Met0p 0006 09

Packaging label for Metoclopramide Injection, USP, 10 mg/2 mL (5 mg/mL) solution. The label indicates the product contains 24 prefilled 2 mL single-use syringes intended for intravenous or intramuscular use. The labeler is Fresenius Kabi USA, LLC. The packaging includes usage and handling instructions and barcode.*

FDA Label Image

Met0p 0006 10

Label for Metoclopramide Injection, USP 10 mg/2 mL (5 mg/mL) single-use prefilled syringe by Fresenius Kabi USA, LLC. The label indicates it is for intravenous or intramuscular use and includes storage instructions, lot number, expiration date placeholders, and a barcode.*

FDA Label Image

Met0p 0006 11

Label for Metoclopramide 10 mg/2 mL injection, USP, indicated for intravenous or intramuscular use. The label shows dosing volume markings from 0.5 mL to 2 mL with a barcode and the labeler name Fresenius Kabi USA, LLC. The concentration is noted as 5 mg/mL with a single-use instruction.*

* 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.