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  5. NDC Package Code: 59999-001-04 Childrens Acetaminophen

NDC Package 59999-001-04 Childrens Acetaminophen

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
59999-001-04
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
59999-001
Proprietary Name:
Childrens Acetaminophen
Usage Information:
Do not give more than directed (see Liver and overdose warning)shake well before usethis product does not contain directions or complete warnings for adult useuse only with enclosed dosing cuprepeat dose every 4 hours if neededdo not give more than 5 times in 24 hoursdo not give for more than 5 days unless directed by a doctorfind right dose on chart below. If possible, use weight to dose, otherwise; use age.Weight (lb)Age (yr)Dose (tsp or mL)under 24under 2 yearsask a doctor24-352-3 years1 tsp or 5 mL36-474-5 years1 1/2 tsp or 7.5 mL48-596-8 years2 tsp or 10 mL60-719-10 years2 1/2 tsp or 12.5 mL72-9511 years3 tsp or 15 mL
11-Digit NDC Billing Format:
59999000104
NDC to RxNorm Crosswalk:
  • RxCUI: 307668 - acetaminophen 160 MG in 5 mL Oral Suspension
  • RxCUI: 307668 - acetaminophen 32 MG/ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 160 MG per 5 ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 320 MG per 10 ML Oral Suspension
  • RxCUI: 307668 - acetaminophen 650 MG per 20.3 ML Oral Suspension
    • Labeler Name:
    R3 Pharmaceuticals, Llc
    Sample Package:
    No
    Start Marketing Date:
    09-23-2013
    Listing Expiration Date:
    12-31-2017
    Exclude Flag:
    I
    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 59999-001-04?

    The NDC Packaged Code 59999-001-04 is assigned to a package of 1 bottle, plastic in 1 carton / 118 ml in 1 bottle, plastic of Childrens Acetaminophen, labeled by R3 Pharmaceuticals, Llc. The product's dosage form is and is administered via form.

    Is NDC 59999-001 included in the NDC Directory?

    No, Childrens Acetaminophen with product code 59999-001 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by R3 Pharmaceuticals, Llc on September 23, 2013 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 59999-001-04?

    The 11-digit format is 59999000104. 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
    5-3-259999-001-045-4-259999-0001-04