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  5. NDC Package Code: 70934-854-30 Diltiazem Hydrochloride

NDC Package 70934-854-30 Diltiazem Hydrochloride

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
70934-854-30
Package Description:
30 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70934-854
Proprietary Name:
Diltiazem Hydrochloride
Non-Proprietary Name:
Diltiazem Hydrochloride
Substance Name:
Diltiazem Hydrochloride
Usage Information:
Diltiazem hydrochloride tablets are indicated for the management of chronic stable angina and angina due to coronary artery spasm.
11-Digit NDC Billing Format:
70934085430
NDC to RxNorm Crosswalk:
  • RxCUI: 831103 - dilTIAZem hydrochloride 60 MG Oral Tablet
  • RxCUI: 831103 - diltiazem hydrochloride 60 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Denton Pharma, Inc. Dba Northwind Pharmaceuticals
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DILTIAZEM HYDROCHLORIDE 60 mg/1
    • Pharmacologic Class(es):
  • Calcium Channel Antagonists - [MoA] (Mechanism of Action)
  • Calcium Channel Blocker - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA018602
    Marketing Category:
    NDA AUTHORIZED GENERIC - A product marketed as a "generic" drug under an approved New Drug Application (NDA), rather than an Abbreviated New Drug Application (ANDA),.
    Start Marketing Date:
    04-23-2021
    End Marketing Date:
    05-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 70934-854-30?

    The NDC Packaged Code 70934-854-30 is assigned to a package of 30 tablet in 1 bottle, plastic of Diltiazem Hydrochloride, a human prescription drug labeled by Denton Pharma, Inc. Dba Northwind Pharmaceuticals. The product's dosage form is tablet and is administered via oral form.

    Is NDC 70934-854 included in the NDC Directory?

    Yes, Diltiazem Hydrochloride with product code 70934-854 is active and included in the NDC Directory. The product was first marketed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals on April 23, 2021.

    What is the 11-digit format for NDC 70934-854-30?

    The 11-digit format is 70934085430. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-270934-854-305-4-270934-0854-30