Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 51407-474

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 51407-474). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Golden State Medical Supply, 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

51407-473-90ol.jpg (51407 473 90ol)

Label for Diltiazem Hydrochloride extended-release capsules, USP, 120 mg, with a once-a-day dosage. The label indicates a package size of 90 capsules. It is marked for prescription use only and includes storage instructions, manufacturer (TWi Pharmaceuticals, Inc.), and marketer information (GSMS, Incorporated). The label features the NDC code 51407-473-90 and a GSMS logo.*

FDA Label Image

51407-474-90ol.jpg (51407 474 90ol)

Label for Diltiazem Hydrochloride 180 mg extended-release capsules, USP. The label shows the product name, strength, and dosage form with a package size of 90 capsules, marked Rx only. Manufacturer is TWi Pharmaceuticals, marketed by GSMS Incorporated. The label includes storage instructions and a barcode with NDC 51407-474-90.*

FDA Label Image

51407-475-90ol.jpg (51407 475 90ol)

Label for Diltiazem Hydrochloride extended-release capsules, 240 mg strength, supplied in a container of 90 capsules. The label shows the product name with emphasis on Diltiazem Hydrochloride, indicates once-a-day dosage, and includes storage and dispensing instructions. Manufactured by TWi Pharmaceuticals, Inc. and marketed by GSMS Incorporated.*

FDA Label Image

51407-476-90ol.jpg (51407 476 90ol)

Label for Diltiazem Hydrochloride extended-release capsules, USP, 300 mg strength. The label indicates a once-a-day dosage with a count of 90 capsules. The product is marketed by GSMS, Incorporated and manufactured by TWi Pharmaceuticals, Inc. It includes storage instructions and warnings about humidity and container integrity. The NDC number is 51407-476-90.*

FDA Label Image

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FDA Label Image

03aa71a-dcc0-4a41-815d-42293e69e7a8 (D03aa71a Dcc0 4a41 815d 42293e69e7a8)

Chemical structure of Diltiazem hydrochloride depicted as a 2D molecular diagram showing its atomic composition and bonds, including the hydrochloride (HCl) component.*

* 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.