Phenylephrine Hydrochloride Injection
Product Images NDC 71872-7159

3 FDA label images from Medical Purchasing Solutions, Llc · 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 Phenylephrine Hydrochloride (NDC 71872-7159). 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

71872-7159-1 Pdp (71872 7159 1 Pdp)

71872-7159-1 Pdp (71872 7159 1 Pdp)
Label for Phenylephrine Hydrochloride Injection, USP 10 mg/mL single-dose vial for intravenous use. The label includes storage instructions, ingredients per mL, and manufacturer information: Amneal Pharmaceuticals Pvt Ltd and Medical Purchasing Solutions, LLC. The label also states dilution, protection from light, and repackaging details.*
FDA Label Image

1 (Phenylephrine Hydrochloride 1 mL 1)

1 (Phenylephrine Hydrochloride 1 mL 1)
Chemical structure diagram of phenylephrine hydrochloride showing its molecular arrangement including a benzene ring, hydroxyl groups, an amine group, and hydrochloride moiety.*
FDA Label Image

1 (Phenylephrine Hydrochloride 1 mL 2)

1 (Phenylephrine Hydrochloride 1 mL 2)
Phenylephrine Hydrochloride Injection, USP 10 mg/mL for intravenous use. The label indicates it is a 1 mL single-dose vial that must be diluted before use, marked as Rx only. Manufactured by Modi Infotex in India and distributed by Amanana Biosciences LLC, Bridgewater, NJ 08807. Storage instructions specify protecting from light and keeping controlled room temperature (59 to 86°F).*

* 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.