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  5. NDC Package Code: 73300-0003-1 Stamina

NDC Package 73300-0003-1 Stamina

Calcarea Fluorica,Calcarea Phosphorica,Calcarea Sulphurica,Ferrum Phosphoricum,Kali - 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:
73300-0003-1
Package Description:
120 TABLET in 1 BOTTLE
Product Code:
73300-0003
Proprietary Name:
Stamina
Non-Proprietary Name:
Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Ferrum Phosphoricum, Kali Muriaticum, Kali Phosphoricum, Kari Sulphuricum, Magnesia Phosphorica, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Silicea
Substance Name:
Calcium Fluoride; Calcium Sulfate Anhydrous; Dibasic Potassium Phosphate; Ferrosoferric Phosphate; Magnesium Phosphate, Dibasic Trihydrate; Potassium Chloride; Potassium Sulfate; Silicon Dioxide; Sodium Chloride; Sodium Phosphate, Dibasic, Heptahydrate; Sodium Sulfate; Tribasic Calcium Phosphate
Usage Information:
Combat depletion or dehydration, rebuild or retain stable energy levels. If you're running on empty...or you want to make sure you aren't...nourish with this stuff. Combat depletion or dehydration, rebuild or retain stable energy levels. If you're running on empty...or you want to make sure you aren't...nourish with this stuff.
11-Digit NDC Billing Format:
73300000301
Product Type:
Human Otc Drug
Labeler Name:
Spirit Homeopathy Llc
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):
  • CALCIUM FLUORIDE 12 [hp_C]/1
  • CALCIUM SULFATE ANHYDROUS 12 [hp_C]/1
  • DIBASIC POTASSIUM PHOSPHATE 12 [hp_C]/1
  • FERROSOFERRIC PHOSPHATE 12 [hp_C]/1
  • MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE 12 [hp_C]/1
  • POTASSIUM CHLORIDE 12 [hp_C]/1
  • POTASSIUM SULFATE 12 [hp_C]/1
  • SILICON DIOXIDE 12 [hp_C]/1
  • SODIUM CHLORIDE 12 [hp_C]/1
  • SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE 12 [hp_C]/1
  • SODIUM SULFATE 12 [hp_C]/1
  • TRIBASIC CALCIUM PHOSPHATE 12 [hp_C]/1
    • Pharmacologic Class(es):
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Blood Coagulation Factor - [EPC] (Established Pharmacologic Class)
  • Calcium - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cations, Divalent - [CS]
  • Increased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • 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)
  • Phosphate Binder - [EPC] (Established Pharmacologic Class)
  • Phosphate Chelating Activity - [MoA] (Mechanism of Action)
  • Potassium Compounds - [CS]
  • Potassium Salt - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    08-12-2020
    End Marketing Date:
    08-19-2025
    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 73300-0003-1?

    The NDC Packaged Code 73300-0003-1 is assigned to a package of 120 tablet in 1 bottle of Stamina, a human over the counter drug labeled by Spirit Homeopathy Llc. The product's dosage form is tablet and is administered via oral form.

    Is NDC 73300-0003 included in the NDC Directory?

    Yes, Stamina with product code 73300-0003 is active and included in the NDC Directory. The product was first marketed by Spirit Homeopathy Llc on August 12, 2020.

    What is the 11-digit format for NDC 73300-0003-1?

    The 11-digit format is 73300000301. 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
    5-4-173300-0003-15-4-273300-0003-01