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  5. NDC Package Code: 48951-6011-4 Kali Phos. Aurum

NDC Package 48951-6011-4 Kali Phos. Aurum

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:
48951-6011-4
Package Description:
250 TABLET in 1 BOTTLE, GLASS
Product Code:
48951-6011
Proprietary Name:
Kali Phos. Aurum
Non-Proprietary Name:
Kali Phos. Aurum
Substance Name:
Ferrous Sulfate; Gold; Potassium Phosphate, Monobasic; Silicon Dioxide
Usage Information:
Directions: FOR ORAL USE ONLY.
11-Digit NDC Billing Format:
48951601104
Product Type:
Human Otc Drug
Labeler Name:
Uriel Pharmacy Inc.
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):
  • FERROUS SULFATE 5 [hp_X]/1
  • GOLD 10 [hp_X]/1
  • POTASSIUM PHOSPHATE, MONOBASIC 6 [hp_X]/1
  • SILICON DIOXIDE 5 [hp_X]/1
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    09-01-2009
    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 48951-6011-4?

    The NDC Packaged Code 48951-6011-4 is assigned to a package of 250 tablet in 1 bottle, glass of Kali Phos. Aurum, a human over the counter drug labeled by Uriel Pharmacy Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 48951-6011 included in the NDC Directory?

    Yes, Kali Phos. Aurum with product code 48951-6011 is active and included in the NDC Directory. The product was first marketed by Uriel Pharmacy Inc. on September 01, 2009 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 48951-6011-4?

    The 11-digit format is 48951601104. 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
    5-4-148951-6011-45-4-248951-6011-04