Hydromorphone Hydrochloride Injection, Solution
Product Images NDC 63323-853

Product Visual Gallery

This gallery contains 14 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 63323-853). 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

Hydro-struc-01.jpg (Hydro Struc 01)

Chemical structure of Hydromorphone Hydrochloride showing the molecular arrangement with hydroxyl, methyl, and ketone functional groups and the hydrochloride component.*

FDA Label Image

Hydro-img-01.jpg (Hydro Img 01)

FDA Label Image

Hydro-label-01.jpg (Hydro Label 01)

Label for Hydromorphone Hydrochloride Injection, USP 1 mg/mL solution in a 1 mL single-dose vial. The label indicates intramuscular, intravenous, or subcutaneous use, and notes the product is preservative free and should be protected from light. Manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

Hydro-label-02.jpg (Hydro Label 02)

Hydromorphone Hydrochloride Injection, USP 1 mg/mL single-dose vials, 25 vials per package. The label indicates the product is preservative-free for intramuscular, intravenous, or subcutaneous use. It is labeled by Fresenius Kabi USA, LLC. Storage instructions are 20° to 25°C with protection from light. The package includes relevant dosing and handling information.*

FDA Label Image

Hydro-label-03.jpg (Hydro Label 03)

Hydromorphone Hydrochloride Injection, USP 2 mg per mL single dose vial label. The label indicates preservative-free solution for intramuscular, intravenous, or subcutaneous use. The labeler is Fresenius Kabi USA, LLC. The label includes NDC 63323-853-03, barcode, lot/expiration area, and dosage form information.*

FDA Label Image

Hydro-label-04.jpg (Hydro Label 04)

Hydromorphone Hydrochloride Injection, USP 2 mg per mL in a 25 x 1 mL single-dose vial package. The label states it is preservative free and for intramuscular, intravenous, or subcutaneous use. Manufactured by Fresenius Kabi USA, LLC, Lake Zurich, IL. The label includes storage instructions (20° to 25°C) and notes the vial closure does not contain natural rubber latex.*

FDA Label Image

Hydro-label-05.jpg (Hydro Label 05)

Label for Hydromorphone Hydrochloride Injection, USP 4 mg per mL in a 1 mL single dose vial. The injection is preservative free and indicated for intramuscular, intravenous, or subcutaneous use. The label displays the NDC 63323-854-03 and is manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

Hydro-label-06.jpg (Hydro Label 06)

Hydromorphone Hydrochloride Injection, USP, 4 mg per mL single-dose vials. The label states it is preservative-free and intended for intramuscular, intravenous, or subcutaneous use. The package contains 25 vials of 1 mL each. It is labeled by Fresenius Kabi USA, LLC, with storage instructions between 20° to 25°C and warnings about protecting from light and discarding unused portions.*

FDA Label Image

Hydro-label-07.jpg (Hydro Label 07)

Label for Hydromorphone Hydrochloride Injection, USP 10 mg per mL, a high potency formula. The label indicates it is preservative free, for single dose vial use of 1 mL, and is intended for prescription use only. The label shows the manufacturer Fresenius Kabi and includes a barcode and NDC 63323-851-03.*

FDA Label Image

Hydro-label-08.jpg (Hydro Label 08)

Label for Hydromorphone Hydrochloride Injection, USP 10 mg per mL by Fresenius Kabi USA, LLC. The label states it is preservative free, Rx only, packaged as 10 single dose vials of 1 mL each. It includes storage instructions (20-25°C), contents of each mL, and a barcode.*

FDA Label Image

Hydro-label-09.jpg (Hydro Label 09)

Label for Hydromorphone Hydrochloride Injection, USP, 10 mg/mL concentration, 5 mL single dose vial. The label states it is preservative free and intended for preparation of large-volume parenteral solutions. It includes storage instructions (20° to 25°C) and notes Fresenius Kabi as the labeler.*

FDA Label Image

Hydro-label-10.jpg (Hydro Label 10)

Label for Hydromorphone Hydrochloride Injection, USP, 10 mg/mL (50 mg per 5 mL) in single-dose vials, 10 x 5 mL, preservative free. The label includes directions for storage at controlled room temperature and states the product is for Rx only. It is supplied by Fresenius Kabi USA, LLC, Lake Zurich, IL.*

FDA Label Image

Hydro-label-11.jpg (Hydro Label 11)

Label for Hydromorphone Hydrochloride Injection, USP 10 mg/mL (500 mg/50 mL) by Fresenius Kabi USA, LLC. It is a single-dose vial with a high potency formula for preparation of large-volume parenteral solutions. The label includes preservative-free status, active ingredient concentration, excipients, storage instructions, and usage notes.*

FDA Label Image

Hydro-label-12.jpg (Hydro Label 12)

The packaging label for Hydromorphone Hydrochloride Injection, USP, displays a strength of 500 mg per 50 mL (10 mg per mL). The label includes regulatory and storage information, stating it is a high potency formula for preparation of large-volume parenteral solutions, preservative-free, and requires storing at controlled room temperature. The product is a single-dose vial, distributed by Fresenius Kabi USA, LLC, and includes cautionary details about the container closure and composition of the solution.*

* 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.