Diltiazem Hydrochloride Injection
Product Images NDC 0641-9219

8 FDA label images from Hikma Pharmaceuticals Usa Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 0641-9219). 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 HCl Injection Novaplus 1)

Diltiazem Hydrochloride Structural Formula (Diltiazem HCl Injection   Novaplus 1)
Chemical structure of Diltiazem Hydrochloride showing its molecular arrangement including aromatic rings, sulfur, nitrogen, and functional groups including methyl and acetoxy groups, with the hydrochloride indicated.*
FDA Label Image

New Logo (Diltiazem HCl Injection Novaplus 2)

New Logo (Diltiazem HCl Injection   Novaplus 2)
Label for Diltiazem Hydrochloride Injection 25 mg per 5 mL (5 mg/mL) by Hikma Pharmaceuticals USA Inc. The 5 mL single-dose vial is for direct IV bolus injection and continuous IV infusion. The label includes dosage instructions, storage conditions (refrigeration 2° to 8°C), and a barcode.*
FDA Label Image

5 mL Vial Container (Diltiazem HCl Injection Novaplus 3)

5 mL Vial Container (Diltiazem HCl Injection   Novaplus 3)
Label for Diltiazem Hydrochloride Injection 25 mg per 5 mL (5 mg/mL) by Hikma Pharmaceuticals USA Inc. It is for intravenous use, available as 10 single-dose vials of 5 mL each, for bolus injection and continuous intravenous infusion. The label includes storage instructions, stating to store refrigerated between 2 to 8°C (36 to 46°F) and not to freeze, with discard instructions for unused portions.*
FDA Label Image

5 mL Vial X 10 Shelfpack (Diltiazem HCl Injection Novaplus 4)

5 mL Vial X 10 Shelfpack (Diltiazem HCl Injection   Novaplus 4)
Label for Diltiazem Hydrochloride Injection 5 mg/mL (50 mg per 10 mL) single dose vial, indicated for intravenous use including direct IV bolus and continuous IV infusion. The label includes storage instructions at 2° to 8°C, non-latex sterile vial designation, manufacturer Hikma Pharmaceuticals USA Inc., and barcode details.*
FDA Label Image

10 mL Vial Novaplus (Diltiazem HCl Injection Novaplus 5)

10 mL Vial Novaplus (Diltiazem HCl Injection   Novaplus 5)
Diltiazem Hydrochloride Injection label for intravenous use, 50 mg per 10 mL (5 mg/mL) strength. The label indicates 10 single-dose vials of 10 mL each, manufactured by Hikma Pharmaceuticals USA Inc. It includes dosage instructions and storage conditions, emphasizing refrigeration and single-dose use. The label also features branding from NovaPlus.*
FDA Label Image

10 mL Vial X 10 Novaplus (Diltiazem HCl Injection Novaplus 6)

10 mL Vial X 10 Novaplus (Diltiazem HCl Injection   Novaplus 6)
Diltiazem Hydrochloride Injection 125 mg per 25 mL (5 mg/mL) single-dose vial label from Hikma Pharmaceuticals USA Inc. for intravenous use. The label includes dosage and storage instructions, barcode, lot, and expiration date areas. It is intended for IV bolus injection and continuous IV infusion.*
FDA Label Image

25 mL Vial Novaplus (Diltiazem HCl Injection Novaplus 7)

25 mL Vial Novaplus (Diltiazem HCl Injection   Novaplus 7)
Diltiazem Hydrochloride Injection 5 mg/mL in a 25 mL single-dose vial. The label states it is for direct intravenous bolus injection and continuous intravenous infusion. The packaging is marked for Rx use only and contains 10 single-dose vials. The labeler is Hikma Pharmaceuticals USA Inc.*
FDA Label Image

10 X 25 mL Shelfpack Novaplus (Diltiazem HCl Injection Novaplus 8)

10 X 25 mL Shelfpack Novaplus (Diltiazem HCl Injection   Novaplus 8)
The image shows a drug label containing a QR code and alphanumeric batch and product information. Visible text includes GTIN 00301234567896, serial number 1234567890123, placeholders for expiry date (EXP MMYYYY), and lot number ABCDE12345. The label does not display the product name, strength, or manufacturer.*

* 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.