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  5. NDC Package Code: 63323-714-14 Perikabiven

NDC Package 63323-714-14 Perikabiven

Dextrose,Soybean - 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:
63323-714-14
Package Description:
1440 mL in 1 BAG
Product Code:
63323-714
Proprietary Name:
Perikabiven
Non-Proprietary Name:
Dextrose, Soybean Oil, Electrolytes, Lysine, Phenylalanine, Leucine, Valine, Threonine, Methionine, Isoleucine, Tryptophan, Alanine, Arginine, Glycine, Proline, Histidine, Glutamic Acid, Serine, Aspartic Acid And Tyrosine
Substance Name:
Alanine; Arginine; Aspartic Acid; Calcium Chloride; Dextrose Monohydrate; Glutamic Acid; Glycine; Histidine; Isoleucine; Leucine; Lysine Hydrochloride; Magnesium Sulfate Heptahydrate; Methionine; Phenylalanine; Potassium Chloride; Proline; Serine; Sodium Acetate; Sodium Glycerophosphate Anhydrous; Soybean Oil; Threonine; Tryptophan; Tyrosine; Valine
Usage Information:
PERIKABIVEN® is indicated as a source of calories, protein, electrolytes and essential fatty acids for adult patients requiring parenteral nutrition when oral or enteral nutrition is not possible, insufficient, or contraindicated.  PERIKABIVEN® may be used to prevent essential fatty acid deficiency or treat negative nitrogen balance in adult patients. Limitations of Use:PERIKABIVEN® is not recommended for use in pediatric patients under the age of 2 years, including preterm infants because the fixed content of the formulation does not meet the nutritional requirements of this age group [see Warnings and Precautions (5.1) and Use in Specific Populations (8.4)].
11-Digit NDC Billing Format:
63323071414
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
1440 ML
Product Type:
Human Prescription Drug
Labeler Name:
Fresenius Kabi Usa, Llc
Dosage Form:
Injection, Emulsion - An emulsion consisting of a sterile, pyrogen-free preparation intended to be administered parenterally.
Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • ALANINE 333 mg/100mL
  • ARGININE 235 mg/100mL
  • ASPARTIC ACID 71 mg/100mL
  • CALCIUM CHLORIDE 20 mg/100mL
  • DEXTROSE MONOHYDRATE 7.5 g/100mL
  • GLUTAMIC ACID 116 mg/100mL
  • GLYCINE 164 mg/100mL
  • HISTIDINE 141 mg/100mL
  • ISOLEUCINE 116 mg/100mL
  • LEUCINE 164 mg/100mL
  • LYSINE HYDROCHLORIDE 187 mg/100mL
  • MAGNESIUM SULFATE HEPTAHYDRATE 68 mg/100mL
  • METHIONINE 116 mg/100mL
  • PHENYLALANINE 164 mg/100mL
  • POTASSIUM CHLORIDE 124 mg/100mL
  • PROLINE 141 mg/100mL
  • SERINE 94 mg/100mL
  • SODIUM ACETATE 170 mg/100mL
  • SODIUM GLYCEROPHOSPHATE ANHYDROUS 105 mg/100mL
  • SOYBEAN OIL 3.5 g/100mL
  • THREONINE 116 mg/100mL
  • TRYPTOPHAN 40 mg/100mL
  • TYROSINE 4.8 mg/100mL
  • VALINE 152 mg/100mL
    • Pharmacologic Class(es):
  • Amino Acid - [EPC] (Established Pharmacologic Class)
  • Amino Acids - [CS]
  • 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)
  • Lipid Emulsion - [EPC] (Established Pharmacologic Class)
  • Lipids - [CS]
  • 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
    FDA Application Number:
    NDA200656
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    08-25-2014
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    63323-714-191920 mL in 1 BAG

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 63323-714-14?

    The NDC Packaged Code 63323-714-14 is assigned to a package of 1440 ml in 1 bag of Perikabiven, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is injection, emulsion and is administered via intravenous form.This product is billed per "ML" milliliter and contains an estimated amount of 1440 billable units per package.

    Is NDC 63323-714 included in the NDC Directory?

    Yes, Perikabiven with product code 63323-714 is active and included in the NDC Directory. The product was first marketed by Fresenius Kabi Usa, Llc on August 25, 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 63323-714-14?

    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 1440.

    What is the 11-digit format for NDC 63323-714-14?

    The 11-digit format is 63323071414. 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
    5-3-263323-714-145-4-263323-0714-14