NDC Package 17856-0502-1 Phenobarbital

View Billable Units, 11-Digit Format, RxNorm

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:
17856-0502-1
Package Description:
72 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE / 5 mL in 1 CUP, UNIT-DOSE
Product Code:
Proprietary Name:
Phenobarbital
Usage Information:
This medication is used alone or with other medications to control seizures. Controlling and reducing seizures lets you do more of your normal daily activities, reduces your risk of harm when you lose consciousness, and lessens your risk for a possibly life-threatening condition of frequent, repeated seizures. Phenobarbital belongs to a class of drugs known as barbiturate anticonvulsants/hypnotics. It works by controlling the abnormal electrical activity in the brain that occurs during a seizure. This medication is also used for a short time (usually no more than 2 weeks) to help calm you or help you sleep during periods of anxiety. It works by affecting certain parts of the brain to cause calming.
11-Digit NDC Billing Format:
17856050201
NDC to RxNorm Crosswalk:
  • RxCUI: 702519 - PHENobarbital 20 MG in 5 mL Oral Solution
  • RxCUI: 702519 - phenobarbital 4 MG/ML Oral Solution
  • RxCUI: 702519 - phenobarbital 20 MG per 5 ML Oral Solution
  • RxCUI: 702519 - phenobarbital 30 MG per 7.5 ML Oral Solution
  • RxCUI: 702519 - phenobarbital 60 MG per 15 ML Oral Solution
  • Labeler Name:
    Atlantic Biologicals Corp.
    Sample Package:
    No
    Start Marketing Date:
    04-04-2019
    Listing Expiration Date:
    12-31-2022
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    17856-0502-272 CUP, UNIT-DOSE in 1 CUP, UNIT-DOSE / 7.5 mL in 1 CUP, UNIT-DOSE
    17856-0502-348 SYRINGE in 1 BOX, UNIT-DOSE / 5 mL in 1 SYRINGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 17856-0502-1?

    The NDC Packaged Code 17856-0502-1 is assigned to a package of 72 cup, unit-dose in 1 cup, unit-dose / 5 ml in 1 cup, unit-dose of Phenobarbital, labeled by Atlantic Biologicals Corp.. The product's dosage form is and is administered via form.

    Is NDC 17856-0502 included in the NDC Directory?

    No, Phenobarbital with product code 17856-0502 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Atlantic Biologicals Corp. on April 04, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 17856-0502-1?

    The 11-digit format is 17856050201. 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
    5-4-117856-0502-15-4-217856-0502-01