Diltiazem Hydrochloride Tablet
Product Images NDC 50228-482

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 50228-482). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen Pharmaceuticals, 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 (Diltiazem 01)

Chemical Structure (Diltiazem 01)
Chemical structure of Diltiazem Hydrochloride depicting the arrangement of atoms and bonds including benzene rings, sulfur, and functional groups.*
FDA Label Image

30mg (Label1)

30mg (Label1)
Label for Diltiazem Hydrochloride Tablets USP 30 mg by ScieGen Pharmaceuticals, Inc. The oral tablet package contains 30 tablets and is for prescription use only. The label includes storage instructions, a barcode, and manufacturer information from ScieGen Pharmaceuticals, Inc., Hauppauge, NY.*
FDA Label Image

30mg (Label2)

30mg (Label2)
Label for Diltiazem Hydrochloride Tablets, USP 30 mg oral tablets by ScieGen Pharmaceuticals, Inc. The label shows the NDC 50228-481-10 and states a package size of 1,000 tablets. It includes usage instructions, storage conditions, pharmacist dispensing instructions, warnings, and manufacturing information on the left side.*
FDA Label Image

30mg (Label3)

30mg (Label3)
Label for Diltiazem Hydrochloride Tablets, USP 60 mg, oral tablets. The label indicates a package of 30 tablets, manufactured by ScieGen Pharmaceuticals, Inc. It includes storage instructions and a warning to keep out of reach of children. The label displays the NDC number 50228-482-30 and a barcode.*
FDA Label Image

30mg (Label4)

30mg (Label4)
Label for Diltiazem Hydrochloride Tablets, USP, 60 mg strength. The label states the product contains 1,000 tablets and is for prescription use only. Manufactured by ScieGen Pharmaceuticals, Inc. The label includes dosage form, strength, storage instructions, warnings, and the NDC number 50228-482-10. Barcode and manufacturer logo are also shown.*
FDA Label Image

30mg (Label5)

30mg (Label5)
Label for Diltiazem Hydrochloride Tablets, USP 90 mg, from ScieGen Pharmaceuticals, Inc. The label displays the strength as 90 mg and indicates the package contains 30 tablets. It includes storage instructions, pharmacist dispensing guidance, and manufacturer information.*
FDA Label Image

30mg (Label6)

30mg (Label6)
Diltiazem Hydrochloride Tablets USP 90 mg oral tablets label by ScieGen Pharmaceuticals, Inc. The label indicates the product contains 1,000 tablets for prescription use only. It includes storage instructions, warnings, dosage reference, and states the tablets may be swallowed whole, crushed, or chewed. The NDC 50228-483-10 and barcode are also visible.*
FDA Label Image

30mg (Label7)

30mg (Label7)
Label for Diltiazem Hydrochloride Tablets USP 120 mg by ScieGen Pharmaceuticals, Inc. The label includes the active ingredient amount per tablet, storage instructions, warnings, and a 30-tablet count. It also features the NDC 50228-484-30 and bar code, indicating the product is prescription only.*
FDA Label Image

30mg (Label8)

30mg (Label8)
Label for Diltiazem Hydrochloride Tablets USP 120 mg, featuring dosage and storage information. The label states the tablets may be swallowed whole, crushed, or chewed, and contains 500 tablets. Manufactured by ScieGen Pharmaceuticals, Inc., it includes warnings, pharmacist instructions, and a barcode with NDC 50228-484-05.*

* 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.