Diltiazem Hydrochloride Injection
Product Images NDC 0641-6013

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 0641-6013). 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

Diltiazem Hydrochloride Structural Formula (Diltiazem Hydrochloride Injection 1)

Chemical structure of Diltiazem Hydrochloride showing its molecular components including aromatic rings, methoxy group, acetoxy group, and hydrochloride salt.*

FDA Label Image

West-ward Logo (Diltiazem Hydrochloride Injection 2)

Diltiazem Hydrochloride Injection label showing 25 mg per 5 mL (5 mg/mL) single dose vial for intravenous use, supplied by Hikma Pharmaceuticals USA Inc. The label includes dosage instructions for direct IV bolus and continuous IV infusion, storage directions at 2° to 8°C (36° to 46°F), and a note indicating the vial is non-latex and sterile.*

FDA Label Image

Diltiazem HCl Injection 25 mg/5 mL (5 mg/ml) 5 mL Single Dose Vial (Diltiazem Hydrochloride Injection 3)

Diltiazem Hydrochloride Injection label for 25 mg per 5 mL (5 mg/mL) single-dose vials. The label indicates use for intravenous bolus injection and continuous infusion, includes storage instructions, and states it is manufactured by Hikma Pharmaceuticals USA Inc. The label also notes disposal of unused portions and key formulation components.*

FDA Label Image

Diltiazem HCl Injection 25 mg/5 mL (5 mg/ml) 10 X 5 mL Single Dose Vials (Diltiazem Hydrochloride Injection 4)

Diltiazem Hydrochloride Injection label displaying 50 mg per 10 mL (5 mg/mL) strength for intravenous use. The label indicates the product is a 10 mL single-dose vial for direct IV bolus injection and continuous IV infusion. Manufacturer is Hikma Pharmaceuticals USA Inc. Storage instructions specify refrigeration at 2° to 8°C (36° to 46°F) and the label advises discarding unused portions.*

FDA Label Image

Diltiazem HCl Injection 50 mg/10 mL (5 mg/ml) 10 mL Single Dose Vial (Diltiazem Hydrochloride Injection 5)

Diltiazem HCl Injection 50 mg per 10 mL (5 mg/mL) label for single dose vials for intravenous use. The label indicates it is for direct intravenous bolus injection and continuous intravenous infusion. Manufactured by Hikma Pharmaceuticals USA Inc. The label includes storage and dosing instructions and a barcode.*

FDA Label Image

Diltiazem HCl Injection 50 mg/10 mL (5 mg/ml) 10 X 10 mL Single Dose Vials (Diltiazem Hydrochloride Injection 6)

Diltiazem Hydrochloride Injection 5 mg/mL, 125 mg per 25 mL single dose vial. The label indicates it is for direct intravenous bolus injection and continuous intravenous infusion. Manufactured by Hikma Pharmaceuticals USA Inc. Storage instructions include refrigeration and discarding unused portions.*

FDA Label Image

Diltiazem HCl Injection 125 mg/25 mL (5 mg/ml) 25 mL Single Dose Vial (Diltiazem Hydrochloride Injection 7)

Label for Diltiazem HCl Injection, 125 mg per 25 mL (5 mg/mL), an intravenous injection by Hikma Pharmaceuticals USA Inc. It is supplied in 10 single-dose vials each containing 25 mL. The label includes storage instructions, ingredients, and dosage form details.*

FDA Label Image

Diltiazem HCl Injection 125 mg/25 mL (5 mg/ml) 10 X 25 mL Single Dose Vials (Diltiazem Hydrochloride Injection 8)

A product label featuring a QR code and alphanumeric codes including GTIN, serial number (SN), expiration date (EXP), and lot number (LOT). The label corresponds to Diltiazem Hydrochloride injection 5 mg/mL by Hikma Pharmaceuticals USA Inc. The codes provide product identification and traceability information.*

* 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.