Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 48433-030

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 48433-030). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safecor Health Llc, 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

Unit Carton (Unit Carton)

Unit Carton (Unit Carton)
Packaging label for Diltiazem Hydrochloride extended-release capsules distributed by Safecor Health LLC. The label features the UDL logo and indicates the packaging is a unit dose designed for institutional use only. It includes warnings about child safety, light resistance of the container, and advises to check the lot number and expiration date through a window.*
FDA Label Image

Diltiazem Hydrochloride Structural Formula (Image 01)

Diltiazem Hydrochloride Structural Formula (Image 01)
Chemical structure of diltiazem hydrochloride, showing its molecular framework including aromatic rings, methoxy, acetoxy groups, and the hydrochloride salt.*
FDA Label Image

Diltiazem HCl 60 mg Extended-release Capsules, Usp Unit Carton Label (Image 02)

Diltiazem HCl 60 mg Extended-release Capsules, Usp Unit Carton Label (Image 02)
Label for Diltiazem Hydrochloride 60 mg extended-release capsules by Safecor Health LLC. The label indicates a twice-a-day dosage and contains 100 capsules (10 x 10). It notes the active ingredient as diltiazem hydrochloride, equivalent to 55.1 mg diltiazem, with storage instructions and manufacturer information for Mylan Pharmaceuticals Inc.*
FDA Label Image

Diltiazem HCl 90 mg Extended-release Capsules, Usp Unit Carton Label (Image 03)

Diltiazem HCl 90 mg Extended-release Capsules, Usp Unit Carton Label (Image 03)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 90 mg, marketed by Safecor Health LLC under labeler Mylan Pharmaceuticals Inc. The label indicates a twice-a-day dosage with 100 capsules per bottle. It includes storage instructions and a note that each capsule contains 90 mg of diltiazem hydrochloride equivalent to 82.7 mg diltiazem.*
FDA Label Image

Diltiazem HCl 120 mg Extended-release Capsules, Usp Unit Carton Label (Image 05)

Diltiazem HCl 120 mg Extended-release Capsules, Usp Unit Carton Label (Image 05)
Label for Diltiazem Hydrochloride 120 mg extended-release oral capsules by Safecor Health LLC. The label indicates a twice-a-day dosage with 100 capsules (10x10) per bottle, referencing National Drug Code (NDC) 48433-032-20. It includes storage instructions and manufacturer information for Mylan Pharmaceuticals Inc.*
FDA Label Image

Unit Carton (Image 06)

Unit Carton (Image 06)
Packaging label for Diltiazem Hydrochloride extended-release capsules distributed by Safecor Health LLC. The label notes that the unit dose package is not child resistant, intended for institutional use only, and provides storage and safety instructions including keeping out of reach of children and light resistance of the container. The Safecor Health logo and contact information are also displayed.*
FDA Label Image

Unit Carton (Image 07)

Unit Carton (Image 07)
Packaging label for Diltiazem Hydrochloride extended-release capsules by Safecor Health LLC. The label features the UDL logo with the text "A Safecor Health Company". It includes warnings about the unit dose package not being child resistant, intended for institutional use only, and instructions to keep out of children's reach. The label also mentions light-resistance of the container, and a window for viewing lot number and expiration date. Contact information for Safecor Health is provided.*

* 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.