Diltiazem Hydrochloride Capsule, Coated, Extended Release
Product Images NDC 60687-206

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 60687-206). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

120 mg Diltiazem Hydrochloride Extended-release Capsule Blister (120 mg Blister)

120 mg Diltiazem Hydrochloride Extended-release Capsule Blister (120 mg Blister)
Packaging label for Diltiazem Hydrochloride Extended-Release 120 mg capsules, USP (Once-a-Day Dosage). The label includes the product name, strength, capsule form, lot number 123456, and expiration date 03/16. It is labeled by American Health Packaging and shown multiple times on the sheet.*
FDA Label Image

120 mg Diltiazem Hydrochloride Extended-release Capsules Carton (120 mg Carton 0222)

120 mg Diltiazem Hydrochloride Extended-release Capsules Carton (120 mg Carton 0222)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP, 120 mg strength, packaged as 100 capsules (10 x 10). The label includes dosage form and strength, NDC number 60687-195-01, barcode, storage instructions, usage warnings, and distribution by American Health Packaging, Columbus, Ohio.*
FDA Label Image

180 mg Diltiazem Hydrochloride Er Capsules Blister (180 mg Blister)

180 mg Diltiazem Hydrochloride Er Capsules Blister (180 mg Blister)
Label sheet containing multiple labels for Diltiazem Hydrochloride Extended-Release Capsules USP 180 mg, a once-a-day dosage strength. Each label lists the labeler American Health Packaging, lot number 123456, and expiry date 03/16. Barcodes are present on each label.*
FDA Label Image

180 mg Diltiazem Hydrochloride Er Capsules Carton (180 mg Carton)

180 mg Diltiazem Hydrochloride Er Capsules Carton (180 mg Carton)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP, 180 mg strength. The label indicates a 100-capsule package (10 x 10), with a once-a-day dosage. It includes storage instructions, precautions, and manufacturer information: American Health Packaging, Columbus, Ohio.*
FDA Label Image

240 mg Diltiazem Hydrochloride Extended-release Capsule Blister (240 mg Blister)

240 mg Diltiazem Hydrochloride Extended-release Capsule Blister (240 mg Blister)
Packaging label for Diltiazem Hydrochloride Extended-Release Capsules USP 240 mg, showing multiple labels on a sheet. Each label includes the product name, strength (240 mg), dosage form (extended-release capsule), lot number (123456), expiry date (03/16), and is labeled by American Health Packaging. The label also notes the capsule is for once-a-day dosage.*
FDA Label Image

240 mg Diltiazem Hydrochloride Extended-release Capsules Carton (240 mg Carton)

240 mg Diltiazem Hydrochloride Extended-release Capsules Carton (240 mg Carton)
Label for Diltiazem Hydrochloride Extended-Release Capsules, USP, 240 mg strength. The package contains 100 capsules (10 blister cards of 10 capsules each). The label highlights once-a-day dosage and includes storage instructions, warnings, and manufacturer information from American Health Packaging.*
FDA Label Image

300 mg Diltiazem Hydrochloride Extended-release Capsules Carton (300 mg Carton)

300 mg Diltiazem Hydrochloride Extended-release Capsules Carton (300 mg Carton)
Diltiazem Hydrochloride Extended-Release 300 mg capsules label showing a package of 100 capsules (10 x 10). The label indicates the product is a once-a-day dosage, Rx only, packaged and distributed by American Health Packaging in Columbus, Ohio. The National Drug Code (NDC) is 60687-228-01.*
FDA Label Image

Ahp19501

Ahp19501
Capsule of Diltiazem Hydrochloride Extended-Release imprinted with 'par' on one side and 'C829' on the other. The capsule is gray and opaque, with no visible strength or labeler information. The image matches the product labeler American Health Packaging.*
FDA Label Image

Ahp20601

Ahp20601
Capsule-shaped blue and green extended-release tablets marked with 'par' on the green half and 'C830' on the blue half. These match the description of Diltiazem Hydrochloride Extended-Release capsules from American Health Packaging, available in strengths including 120 mg, 180 mg, 240 mg, and 300 mg.*
FDA Label Image

Ahp21701

Ahp21701
Diltiazem Hydrochloride Extended-Release 180 mg capsule imprinted with 'par C831'. The capsule is green with black imprinting. Labeler is American Health Packaging.*
FDA Label Image

Ahp22801

Ahp22801
Capsule-shaped extended-release tablet imprinted with 'par' on the teal half and 'C832' on the white half. This capsule corresponds to Diltiazem Hydrochloride Extended-Release in one of its available strengths, labeled by American Health Packaging. The capsule is half teal and half white in color.*
FDA Label Image

Structural Formula (Structure)

Structural Formula (Structure)
Chemical structure diagram of diltiazem hydrochloride, the active ingredient in Diltiazem Hydrochloride Extended-Release products by American Health Packaging. The structure includes aromatic rings and functional groups characteristic of this compound.*
FDA Label Image

300 mg Diltiazem Hydrochloride Extended-release Capsule Blister (Image 01)

300 mg Diltiazem Hydrochloride Extended-release Capsule Blister (Image 01)
Labels for Diltiazem Hydrochloride Extended-Release Capsule, USP 300 mg, once-a-day dosage. Each label includes the proprietary name, strength, dosage form, labeler American Health Packaging, a barcode, lot and expiry date fields, and the company address in Columbus, Ohio. Multiple identical labels are shown arranged in a grid.*

* 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.