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  5. NDC Package Code: 68071-5200-3 Dicyclomine Hydrochloride

NDC Package 68071-5200-3 Dicyclomine Hydrochloride

Capsule 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:
68071-5200-3
Package Description:
30 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
68071-5200
Proprietary Name:
Dicyclomine Hydrochloride
Non-Proprietary Name:
Dicyclomine Hydrochloride
Substance Name:
Dicyclomine Hydrochloride
Usage Information:
Dicyclomine hydrochloride capsules, USP are indicated for the treatment of patients with functional bowel/irritable bowel syndrome.
11-Digit NDC Billing Format:
68071520003
NDC to RxNorm Crosswalk:
  • RxCUI: 991061 - dicyclomine HCl 10 MG Oral Capsule
  • RxCUI: 991061 - dicyclomine hydrochloride 10 MG Oral Capsule
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Nucare Pharmaceuticals,inc.
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • DICYCLOMINE HYDROCHLORIDE 10 mg/1
    • Pharmacologic Class(es):
  • Anticholinergic - [EPC] (Established Pharmacologic Class)
  • Cholinergic Antagonists - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    ANDA040204
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    02-28-1997
    Listing Expiration Date:
    12-31-2024
    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 68071-5200-3?

    The NDC Packaged Code 68071-5200-3 is assigned to a package of 30 capsule in 1 bottle, plastic of Dicyclomine Hydrochloride, a human prescription drug labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is capsule and is administered via oral form.

    Is NDC 68071-5200 included in the NDC Directory?

    Yes, Dicyclomine Hydrochloride with product code 68071-5200 is active and included in the NDC Directory. The product was first marketed by Nucare Pharmaceuticals,inc. on February 28, 1997 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 68071-5200-3?

    The 11-digit format is 68071520003. 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 5-4-1 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
    5-4-168071-5200-35-4-268071-5200-03