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  5. NDC Package Code: 70934-757-90 Dicyclomine Hydrochloride

NDC Package 70934-757-90 Dicyclomine 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:
70934-757-90
Package Description:
90 TABLET in 1 BOTTLE, PLASTIC
Product Code:
70934-757
Proprietary Name:
Dicyclomine Hydrochloride
Non-Proprietary Name:
Dicyclomine Hydrochloride
Substance Name:
Dicyclomine Hydrochloride
Usage Information:
Dicyclomine hydrochloride is indicated for the treatment of patients with functional bowel/irritable bowel syndrome.
11-Digit NDC Billing Format:
70934075790
NDC to RxNorm Crosswalk:
  • RxCUI: 991086 - dicyclomine HCl 20 MG Oral Tablet
  • RxCUI: 991086 - dicyclomine hydrochloride 20 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):
  • DICYCLOMINE HYDROCHLORIDE 20 mg/1
    • Pharmacologic Class(es):
  • Anticholinergic - [EPC] (Established Pharmacologic Class)
  • Cholinergic Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA085223
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-28-2021
    End Marketing Date:
    03-31-2025
    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 70934-757-90?

    The NDC Packaged Code 70934-757-90 is assigned to a package of 90 tablet in 1 bottle, plastic of Dicyclomine 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 70934-757 included in the NDC Directory?

    Yes, Dicyclomine Hydrochloride with product code 70934-757 is active and included in the NDC Directory. The product was first marketed by Denton Pharma, Inc. Dba Northwind Pharmaceuticals on September 28, 2021.

    What is the 11-digit format for NDC 70934-757-90?

    The 11-digit format is 70934075790. 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
    5-3-270934-757-905-4-270934-0757-90