Diltiazem Hydrochloride Capsule, Extended Release
Product Images NDC 70436-193

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 70436-193). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Slate Run Pharmaceuticals, 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

120mg-100ct (120mg 100ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, once-a-day dosage. The label indicates it contains 100 capsules and is manufactured by Slate Run Pharmaceuticals, LLC. It includes storage instructions, child-resistant packaging details, and barcode. The product is for prescription use only.*

FDA Label Image

120mg-500ct (120mg 500ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, manufactured by Yichang Humanwell Oral Solid Dosage Plant and distributed by Slate Run Pharmaceuticals, LLC. This label is for a 500-capsule count, once-a-day dosage form. Storage instructions and dispensing details are provided along with a barcode and lot information area.*

FDA Label Image

180mg-100ct (180mg 100ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules, 180 mg, once-a-day dosage, manufactured and distributed by Slate Run Pharmaceuticals, LLC. The label indicates the package contains 100 capsules. It includes storage instructions, dosage information, and child-resistant packaging warnings, along with manufacturer and distributor addresses.*

FDA Label Image

180mg-500ct (180mg 500ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 180 mg by Slate Run Pharmaceuticals, LLC. The label indicates a once-a-day dosage and package size of 500 capsules. Storage instructions and manufacturer/distributor details are included, along with a barcode and warnings about child safety and packaging.*

FDA Label Image

240mg-100ct (240mg 100ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules USP, 240 mg strength, manufactured by Slate Run Pharmaceuticals, LLC. The label indicates a 100 capsule count and displays the NDC 70436-193-01. It includes storage instructions, child-resistant packaging information, and dosage frequency as once-a-day.*

FDA Label Image

240mg-500ct (240mg 500ct)

Label for Diltiazem Hydrochloride Extended-Release Capsules, USP 240 mg by Slate Run Pharmaceuticals. The label indicates once-a-day dosage and a package size of 500 capsules. It includes storage instructions, a barcode, manufacturer details (Yichang Humanwell, China), and child safety warnings.*

FDA Label Image

Diltiazem Hydrochloride Chemical Structure (Diltiazem Hydrochloride Structure)

Chemical structure of Diltiazem Hydrochloride, showing the molecular arrangement including benzene rings, sulfur, nitrogen, oxygen atoms, and functional groups such as methoxy and acetate ester.*

FDA Label Image

Ink1 (Ink1)

Diltiazem Hydrochloride 180 mg extended release capsules in a clear plastic blister pack with white background and blue text. The blister contains 30 capsules arranged in a 3 by 10 grid. Labeling includes the product name, strength, dosage form, and the manufacturer Slate Run Pharmaceuticals, LLC.*

FDA Label Image

Ink2 (Ink2)

Diltiazem Hydrochloride extended release capsules in a blister pack. The blister contains 30 capsules, each appearing elongated with black and white colors. The packaging is labeled with the strength 120 mg and manufactured by Slate Run Pharmaceuticals, LLC. The text on the blister clearly states the product name and strength.*

FDA Label Image

Ink3 (Ink3)

Diltiazem Hydrochloride 180 mg extended release capsule blister pack from Slate Run Pharmaceuticals, LLC. The foil blister card contains 15 green and white capsules, arranged in three rows of five, with printed lot number and expiration date on the foil.*

* 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.