Dopram Injection
Product Images NDC 0641-6018

View Photos of 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 Dopram (NDC 0641-6018). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structural Formula (Dopram 1)

Structural Formula (Dopram 1)
Chemical structure diagram of doxapram hydrochloride monohydrate, showing the molecular arrangement including a piperidine ring and two phenyl groups. The structure is consistent with the active ingredient doxapram hydrochloride from the drug Dopram injection 20 mg/mL by Hikma Pharmaceuticals USA Inc.*
FDA Label Image

West-ward Logo (Dopram 2)

West-ward Logo (Dopram 2)
Dopram Injection label showing doxapram hydrochloride injection, USP 400 mg per 20 mL (20 mg/mL) dosage form for intravenous use. Contains benzyl alcohol as preservative, not for use in neonates. Packaged in a 20 mL multiple dose vial by Hikma Pharmaceuticals USA Inc., Berkeley Heights, NJ. Storage instructions and other details also visible.*
FDA Label Image

Dopram Injection (doxapram Hydrochloride Injection, Usp) 400 mg/20 mL (20 mg/ml) 20 mL Multiple Dose Vial (Dopram 3)

Dopram Injection (doxapram Hydrochloride Injection, Usp) 400 mg/20 mL (20 mg/ml) 20 mL Multiple Dose Vial (Dopram 3)
The image shows a drug label for Dopram Injection containing Doxapram hydrochloride at 20 mg/mL strength. It includes identifying information such as GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The label is from Hikma Pharmaceuticals USA Inc. and is intended for intravenous use.*

* 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.