NDC Package 52083-056-01 Supress-pe Pediatric

Guiafenesin,Phenylephrine Hcl Solution/ Drops Oral - View Billable Units, 11-Digit Format, RxNorm

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:
52083-056-01
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
Proprietary Name:
Supress-pe Pediatric
Non-Proprietary Name:
Guiafenesin, Phenylephrine Hcl
Substance Name:
Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Other information Tamper Evident Feature: Do not use if cap seal is torn, broken or missing. For your protection, this bottle has an imprinted seal around the neck.Store at controlled room temperature 15-30°C (59-86°F).Avoid excessive heat and humidity.
11-Digit NDC Billing Format:
52083005601
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
30 ML
NDC to RxNorm Crosswalk:
  • RxCUI: 824600 - guaiFENesin 50 MG / phenylephrine HCl 2.5 MG in 1 mL Oral Solution
  • RxCUI: 824600 - guaifenesin 50 MG/ML / phenylephrine hydrochloride 2.5 MG/ML Oral Solution
  • RxCUI: 824600 - guaifenesin 50 MG / phenylephrine HCl 2.5 MG per 1 ML Oral Solution
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Kramer Novis
    Dosage Form:
    Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    FDA Application Number:
    part341
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    01-14-2014
    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 52083-056-01?

    The NDC Packaged Code 52083-056-01 is assigned to a package of 30 ml in 1 bottle, dropper of Supress-pe Pediatric, a human over the counter drug labeled by Kramer Novis. The product's dosage form is solution/ drops and is administered via oral form.This product is billed per "ML" milliliter and contains an estimated amount of 30 billable units per package.

    Is NDC 52083-056 included in the NDC Directory?

    Yes, Supress-pe Pediatric with product code 52083-056 is active and included in the NDC Directory. The product was first marketed by Kramer Novis on January 14, 2014 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 52083-056-01?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume. The calculated billable units for this package is 30.

    What is the 11-digit format for NDC 52083-056-01?

    The 11-digit format is 52083005601. 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
    5-3-252083-056-015-4-252083-0056-01