Hydromorphone Hydrochloride Injection, Solution
Product Images NDC 0409-2634

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Hydromorphone Hydrochloride (NDC 0409-2634). 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

Chemical Structure (Hydromorphone 01)

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FDA Label Image

Logo (Hydromorphone 02)

FDA Label Image

Principal Display Panel (1 mL Vial Label)

This is a description of a medication called "Hydromorphone Hydrochloride Injection, USP". The medication comes in a single-dose vial with the National Drug Code (NDC) 0403-2634-10. The medication is a high potency formulation and has a strength of 7.5 milligrams per milliliter. The manufacturer is Hospira, Inc. and it is only available with a prescription. The lot number is indicated as HEHHEAA with an expiration date of DMMMYYYY, but the remaining details are not available due to poor quality.*

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Carton Ndc-0409-2634-01 (Hydromorphone 04)

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Principal Display Panel (5 mL Vial Label)

This is a description of a high potency formulation of Hydromorphone Hydrochloride Injection, USP. It comes in a 5 mL single-dose vial with an NDC code of 0409-2634-25. It is intended for use in the preparation of 50 mg/5 mL large-volume parenteral solutions, with each mL containing 10 mg of the drug. It is distributed by Hospira, Inc. under the LOT/EXP code of HHEHHEHAA and PAA158974.*

FDA Label Image

Principal Display Panel (5 mL Vial Box)

This is a prescription drug that comes in a box with 10 individual 5 mL vials. The drug is Hydromorphone Hydrochloride Injection with a high potency formulation at 50 mg/5 mL (10mg/mL). It is intended for use in the preparation of large-volume parenteral solutions. The drug should be stored at 20 to 25°C (68 to 77°F) and protected from light. The package must not be broken for resale. The carton shows the lot number and expiration date. The usual dose by injection is not mentioned and should be checked through the package insert for full prescribing information. There is no added preservative in each vial.*

FDA Label Image

Principal Display Panel (50 mL Vial Label)

This is a description of a single-dose vial of Hydromorphone Hydrochloride Injection, USP in a high potency formulation of 10 mg/mL for use in the preparation of large-volume parenteral solutions. The vial is distributed by Hospira, Inc. and has an NDC of 0409-2634-50.*

FDA Label Image

Principal Display Panel (50 mL Vial Box)

This seems to be a mixed output that includes some product labeling information for a medication called Hydromorphone Hydrochloride Injection. It includes details such as the dosage, type of container, and recommended storage conditions. However, some parts of the text are unreadable or contain only symbols, making it difficult to provide a full description.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.