Diltiazem Hydrochloride Tablet
Product Images NDC 70771-1932

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diltiazem Hydrochloride (NDC 70771-1932). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

30 mg 100s Label (F63d2c9f F49a 4b36 B25d 6fbe3ab5577f 01)

Diltiazem Hydrochloride Tablets, USP 30 mg oral tablet bottle label by Zydus Lifesciences Limited. Contains 100 tablets and is for prescription use only. The label includes dosing instructions, storage information, child-resistant packaging notice, and manufacturer details. The NDC is 70771-1929-1.*

FDA Label Image

60 mg 100s (F63d2c9f F49a 4b36 B25d 6fbe3ab5577f 02)

Diltiazem Hydrochloride Tablets USP 60 mg oral tablets label showing a bottle container with 100 tablets. The label indicates the product is manufactured by Zydus Lifesciences Limited. Storage instructions and child-resistant packaging information are included, along with the National Drug Code 70771-1930-1. The label includes warnings to keep out of reach of children and directions to see the package insert for dosing.*

FDA Label Image

90 mg 100s (F63d2c9f F49a 4b36 B25d 6fbe3ab5577f 03)

Label for Diltiazem Hydrochloride Tablets USP 90 mg oral tablets. The package contains 100 tablets and is manufactured by Zydus Lifesciences Limited. The label includes dosage instructions, storage conditions, child-resistant packaging notice, and a barcode with NDC 70771-1931-1.*

FDA Label Image

120 mg 100s (F63d2c9f F49a 4b36 B25d 6fbe3ab5577f 04)

Label for Diltiazem Hydrochloride Tablets, USP 120 mg, oral tablets by Zydus Lifesciences Limited. The package contains 100 tablets with NDC 70771-1932-1. The label provides dosage strength, manufacturer details, storage instructions, child-resistant packaging information, and a barcode.*

* 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.