1. Home
  2. Labeler Index
  3. Braintree Laboratories, Inc.
  4. 52268-012
  5. NDC Package Code: 52268-012-01 Suprep Bowel Prep

NDC Package 52268-012-01 Suprep Bowel Prep

Sodium Sulfate,Potassium Sulfate,Magnesium Sulfate Solution, Concentrate 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:
52268-012-01
Package Description:
2 BOTTLE, PLASTIC in 1 CARTON / 177.4 mL in 1 BOTTLE, PLASTIC
Product Code:
52268-012
Proprietary Name:
Suprep Bowel Prep
Non-Proprietary Name:
Sodium Sulfate, Potassium Sulfate, Magnesium Sulfate
Substance Name:
Magnesium Sulfate, Unspecified Form; Potassium Sulfate; Sodium Sulfate
Usage Information:
SUPREP Bowel Prep Kit is indicated for cleansing of the colon as a preparation for colonoscopy in adults.
11-Digit NDC Billing Format:
52268001201
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1001689 - {2 (480 ML) (magnesium sulfate 0.0277 MEQ/ML / potassium sulfate 0.0374 MEQ/ML / sodium sulfate 0.257 MEQ/ML Oral Solution) } Pack
  • RxCUI: 1001689 - 2 (16 OZ magnesium sulfate 1.6 GM / potassium sulfate 3.13 GM / sodium sulfate 17.5 GM Oral Solution) Pack
  • RxCUI: 1001690 - {2 (480 ML) (magnesium sulfate 0.0277 MEQ/ML / potassium sulfate 0.0374 MEQ/ML / sodium sulfate 0.257 MEQ/ML Oral Solution) } Pack [Suprep Bowel Prep Kit]
  • RxCUI: 1001690 - SUPREP BOWEL PREP KIT
  • RxCUI: 1001690 - {2 (16 OZ magnesium sulfate 1.6 GM / potassium sulfate 3.13 GM / sodium sulfate 17.5 GM Oral Solution) } Pack [Suprep Bowel Prep Kit]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Braintree Laboratories, Inc.
    Dosage Form:
    Solution, Concentrate - A liquid preparation (i.e., a substance that flows readily in its natural state) that contains a drug dissolved in a suitable solvent or mixture of mutually miscible solvents; the drug has been strengthened by the evaporation of its nonactive parts.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • MAGNESIUM SULFATE, UNSPECIFIED FORM 1.6 g/mL
  • POTASSIUM SULFATE 3.13 g/mL
  • SODIUM SULFATE 17.5 g/mL
    • Pharmacologic Class(es):
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Increased Large Intestinal Motility - [PE] (Physiologic Effect)
  • Inhibition Large Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Inhibition Small Intestine Fluid/Electrolyte Absorption - [PE] (Physiologic Effect)
  • Magnesium Ion Exchange Activity - [MoA] (Mechanism of Action)
  • Osmotic Activity - [MoA] (Mechanism of Action)
  • Osmotic Laxative - [EPC] (Established Pharmacologic Class)
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA022372
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-05-2010
    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 52268-012-01?

    The NDC Packaged Code 52268-012-01 is assigned to a package of 2 bottle, plastic in 1 carton / 177.4 ml in 1 bottle, plastic of Suprep Bowel Prep, a human prescription drug labeled by Braintree Laboratories, Inc.. The product's dosage form is solution, concentrate and is administered via oral form.

    Is NDC 52268-012 included in the NDC Directory?

    Yes, Suprep Bowel Prep with product code 52268-012 is active and included in the NDC Directory. The product was first marketed by Braintree Laboratories, Inc. on August 05, 2010 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 NDC billing unit for package 52268-012-01?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 52268-012-01?

    The 11-digit format is 52268001201. 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
    5-3-252268-012-015-4-252268-0012-01