NDC Package 51754-0503-3 Caffeine Citrate

Solution Oral - View Billable Units, 11-Digit Format, RxNorm

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:
51754-0503-3
Package Description:
10 VIAL, SINGLE-DOSE in 1 CONTAINER / 3 mL in 1 VIAL, SINGLE-DOSE
Product Code:
Proprietary Name:
Caffeine Citrate
Non-Proprietary Name:
Caffeine Citrate
Substance Name:
Caffeine Citrate
Usage Information:
This medication is used for the short-term treatment of a breathing problem (apnea) in premature infants. Caffeine blocks certain proteins (adenosine receptors) which lead to improved breathing in these infants.
11-Digit NDC Billing Format:
51754050303
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 849928 - caffeine citrate 60 MG in 3 mL Oral Solution
  • RxCUI: 849928 - caffeine citrate 20 MG/ML Oral Solution
  • RxCUI: 849928 - caffeine citrate 60 MG per 3 ML Oral Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Exela Pharma Sciences, Llc
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    ANDA077304
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    09-21-2006
    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 51754-0503-3?

    The NDC Packaged Code 51754-0503-3 is assigned to a package of 10 vial, single-dose in 1 container / 3 ml in 1 vial, single-dose of Caffeine Citrate, a human prescription drug labeled by Exela Pharma Sciences, Llc. The product's dosage form is solution and is administered via oral form.

    Is NDC 51754-0503 included in the NDC Directory?

    Yes, Caffeine Citrate with product code 51754-0503 is active and included in the NDC Directory. The product was first marketed by Exela Pharma Sciences, Llc on September 21, 2006 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 51754-0503-3?

    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 51754-0503-3?

    The 11-digit format is 51754050303. 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
    5-4-151754-0503-35-4-251754-0503-03