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  5. NDC Package Code: 0642-0207-03 Strovite One Caplets

NDC Package 0642-0207-03 Strovite One Caplets

Vitamin A,Calcium Pantothenate,Ascorbic Acid,Cholecalciferol,.alpha.-tocopherol - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
0642-0207-03
Package Description:
1 BLISTER PACK in 1 BOX / 3 TABLET in 1 BLISTER PACK
Product Code:
0642-0207
Proprietary Name:
Strovite One Caplets
Non-Proprietary Name:
Vitamin A, Calcium Pantothenate, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Succinate, D-, Thiamine, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Biotin, Cyanocobalamin, Selenium, Magnesium Oxide, Zinc Oxide, Cupric Sulfate, Manganese, Chromium, .alpha.-lipoic Acid, And Lutein
Substance Name:
.alpha.-tocopherol Succinate, D-; Alpha Lipoic Acid; Ascorbic Acid; Biotin; Calcium Pantothenate; Cholecalciferol; Chromium; Cupric Sulfate; Cyanocobalamin; Folic Acid; Lutein; Magnesium Oxide; Manganese; Niacinamide; Pyridoxine Hydrochloride; Riboflavin; Selenium; Thiamine; Vitamin A; Zinc Oxide
Usage Information:
This medication is a multivitamin product used to treat or prevent vitamin deficiency due to poor diet, certain illnesses, or during pregnancy. Vitamins are important building blocks of the body and help keep you in good health.
11-Digit NDC Billing Format:
00642020703
Product Type:
Human Prescription Drug
Labeler Name:
Exeltis Usa, 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):
  • .ALPHA.-TOCOPHEROL SUCCINATE, D- 45 ug/1
  • ALPHA LIPOIC ACID 15 mg/1
  • ASCORBIC ACID 300 mg/1
  • BIOTIN 100 ug/1
  • CALCIUM PANTOTHENATE 7.5 mg/1
  • CHOLECALCIFEROL 25 ug/1
  • CHROMIUM 50 ug/1
  • CUPRIC SULFATE 1.5 mg/1
  • CYANOCOBALAMIN 50 ug/1
  • FOLIC ACID 1700 ug/1
  • LUTEIN 5 mg/1
  • MAGNESIUM OXIDE 50 mg/1
  • MANGANESE 1.5 mg/1
  • NIACINAMIDE 25 mg/1
  • PYRIDOXINE HYDROCHLORIDE 25 mg/1
  • RIBOFLAVIN 5 mg/1
  • SELENIUM 100 ug/1
  • THIAMINE 20 mg/1
  • VITAMIN A 900 ug/1
  • ZINC OXIDE 25 mg/1
    • Pharmacologic Class(es):
  • Allergens - [CS]
  • Analogs/Derivatives - [Chemical/Ingredient]
  • Ascorbic Acid - [CS]
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Increased Histamine Release - [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)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Stimulation Large Intestine Fluid/Electrolyte Secretion - [PE] (Physiologic Effect)
  • Vitamin A - [CS]
  • Vitamin A - [EPC] (Established Pharmacologic Class)
  • Vitamin B 12 - [CS]
  • Vitamin B 6 - [Chemical/Ingredient]
  • Vitamin B12 - [EPC] (Established Pharmacologic Class)
  • Vitamin B6 Analog - [EPC] (Established Pharmacologic Class)
  • Vitamin C - [EPC] (Established Pharmacologic Class)
  • Vitamin D - [CS]
  • Vitamin D - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    05-04-2001
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0642-0207-9090 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0642-0207-03?

    The NDC Packaged Code 0642-0207-03 is assigned to a package of 1 blister pack in 1 box / 3 tablet in 1 blister pack of Strovite One Caplets, a human prescription drug labeled by Exeltis Usa, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 0642-0207 included in the NDC Directory?

    Yes, Strovite One Caplets with product code 0642-0207 is active and included in the NDC Directory. The product was first marketed by Exeltis Usa, Inc. on May 04, 2001 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 0642-0207-03?

    The 11-digit format is 00642020703. 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 4-4-2 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
    4-4-20642-0207-035-4-200642-0207-03