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  5. NDC Package Code: 54643-5649-1 Infuvite Adult Multiple Vitamins

NDC Package 54643-5649-1 Infuvite Adult Multiple Vitamins

Ascorbic Acid,Vitamin A Palmitate,Cholecalciferol,Thiamine Hydrochloride,Riboflavin-5 - 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:
54643-5649-1
Package Description:
10 VIAL in 1 CARTON / 5 mL in 1 VIAL
Product Code:
54643-5649
Proprietary Name:
Infuvite Adult Multiple Vitamins
Non-Proprietary Name:
Ascorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin-5 Phosphate Sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol Acetate, Vitamin K1, Folic Acid, Biotin, Cyanocobalamin
Substance Name:
.alpha.-tocopherol Acetate; Ascorbic Acid; Biotin; Cholecalciferol; Cyanocobalamin; Dexpanthenol; Folic Acid; Niacinamide; Phytonadione; Pyridoxine Hydrochloride; Riboflavin 5'-phosphate Sodium; Thiamine Hydrochloride; Vitamin A Palmitate
Usage Information:
INFUVITE ADULT is a combination of vitamins indicated for the prevention of vitamin deficiency in adults and children aged 11 and older receiving parenteral nutrition.The physician should not await the development of clinical signs of vitamin deficiency before initiating vitamin therapy.
11-Digit NDC Billing Format:
54643564901
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1304559 - alpha-tocopherol acetate 1 UNT/ML / ascorbic acid 20 MG/ML / biotin 0.006 MG/ML / cholecalciferol 20 UNT/ML / dexpanthenol 1.5 MG/ML / folic acid 0.06 MG/ML / niacinamide 4 MG/ML / pyridoxine hydrochloride 0.6 MG/ML / riboflavin 0.36 MG/ML / thiamine hydrochloride 0.6 MG/ML / vitamin A palmitate 330 UNT/ML / vitamin B12 0.0005 MG/ML / vitamin K1 0.015 MG/ML Injectable Solution
  • RxCUI: 1304559 - alpha-tocopherol acetate 1 UNT/ML / vitamin C 20 MG/ML / biotin 0.006 MG/ML / cholecalciferol 20 UNT/ML / dexpanthenol 1.5 MG/ML / folate 0.06 MG/ML / niacinamide 4 MG/ML / vitamin B6 hydrochloride 0.6 MG/ML / riboflavin 0.36 MG/ML / vitamin B1 hydrochloride 0.6 MG/ML / vitamin A palmitate 330 UNT/ML / vitamin B12 0.0005 MG/ML / vitamin K1 0.015 MG/ML Injectable Solution
  • RxCUI: 1304559 - alpha-tocopherol acetate 1 UNT/ML / vitamin C 20 MG/ML / biotin 0.006 MG/ML / cholecalciferol 20 UNT/ML / dexpanthenol 1.5 MG/ML / folate 0.06 MG/ML / niacinamide 4 MG/ML / vitamin B6 hydrochloride 0.6 MG/ML / riboflavin 0.36 MG/ML / vit-B1 hydrochloride 0.6 MG/ML / vitamin A palmitate 330 UNT/ML / vitamin B12 0.0005 MG/ML / vitamin K1 0.015 MG/ML Injectable Solution
  • RxCUI: 1304559 - alpha-tocopherol acetate 1 UNT/ML / vitamin C 20 MG/ML / biotin 0.006 MG/ML / cholecalciferol 20 UNT/ML / dexpanthenol 1.5 MG/ML / folate 0.06 MG/ML / niacinamide 4 MG/ML / vit-B6 hydrochloride 0.6 MG/ML / riboflavin 0.36 MG/ML / vitamin B1 hydrochloride 0.6 MG/ML / vitamin A palmitate 330 UNT/ML / vitamin B12 0.0005 MG/ML / vitamin K1 0.015 MG/ML Injectable Solution
  • RxCUI: 1304559 - alpha-tocopherol acetate 1 UNT/ML / vitamin C 20 MG/ML / biotin 0.006 MG/ML / cholecalciferol 20 UNT/ML / dexpanthenol 1.5 MG/ML / folate 0.06 MG/ML / niacinamide 4 MG/ML / vit-B6 hydrochloride 0.6 MG/ML / riboflavin 0.36 MG/ML / vit-B1 hydrochloride 0.6 MG/ML / vitamin A palmitate 330 UNT/ML / vitamin B12 0.0005 MG/ML / vitamin K1 0.015 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Sandoz Inc
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • .ALPHA.-TOCOPHEROL ACETATE 10 [iU]/10mL
  • ASCORBIC ACID 200 mg/10mL
  • BIOTIN 60 ug/10mL
  • CHOLECALCIFEROL 200 [iU]/10mL
  • CYANOCOBALAMIN 5 ug/10mL
  • DEXPANTHENOL 15 mg/10mL
  • FOLIC ACID 600 ug/10mL
  • NIACINAMIDE 40 mg/10mL
  • PHYTONADIONE 150 ug/10mL
  • PYRIDOXINE HYDROCHLORIDE 6 mg/10mL
  • RIBOFLAVIN 5'-PHOSPHATE SODIUM 3.6 mg/10mL
  • THIAMINE HYDROCHLORIDE 6 mg/10mL
  • VITAMIN A PALMITATE 3300 [iU]/10mL
    • Pharmacologic Class(es):
  • Analogs/Derivatives - [Chemical/Ingredient]
  • Ascorbic Acid - [CS]
  • Increased Prothrombin Activity - [PE] (Physiologic Effect)
  • Reversed Anticoagulation Activity - [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)
  • Vitamin K - [CS]
  • Vitamin K - [EPC] (Established Pharmacologic Class)
  • Warfarin Reversal Agent - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA021163
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-18-2005
    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 54643-5649-1?

    The NDC Packaged Code 54643-5649-1 is assigned to a package of 10 vial in 1 carton / 5 ml in 1 vial of Infuvite Adult Multiple Vitamins, a human prescription drug labeled by Sandoz Inc. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 54643-5649 included in the NDC Directory?

    Yes, Infuvite Adult Multiple Vitamins with product code 54643-5649 is active and included in the NDC Directory. The product was first marketed by Sandoz Inc on May 18, 2005 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 54643-5649-1?

    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 54643-5649-1?

    The 11-digit format is 54643564901. 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
    5-4-154643-5649-15-4-254643-5649-01