NDC Package 62756-301-01 Sezaby

Phenobarbital Sodium Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

62756-301-01

Package Description:

1 INJECTION in 1 VIAL, SINGLE-DOSE

Product Code:

62756-301

Proprietary Name:

Sezaby

Non-Proprietary Name:

Phenobarbital Sodium

Substance Name:

Phenobarbital Sodium

Usage Information:

SEZABY is indicated for the treatment of neonatal seizures in term and preterm infants.

11-Digit NDC Billing Format:

62756030101

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

1 EA

NDC to RxNorm Crosswalk:

RxCUI: 2624719 - PHENobarbital sodium 100 MG Injection

RxCUI: 2624719 - phenobarbital sodium 100 MG Injection

RxCUI: 2624724 - Sezaby 100 MG Injection

RxCUI: 2624724 - phenobarbital sodium 100 MG Injection [Sezaby]

Product Type:

Human Prescription Drug

Labeler Name:

Sun Pharmaceutical Industries, Inc.

Dosage Form:

Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.

Administration Route(s):

Intravenous - Administration within or into a vein or veins.

Active Ingredient(s):

PHENOBARBITAL SODIUM 100 mg/1

DEA Schedule:

Schedule IV (CIV) Substances

Sample Package:

FDA Application Number:

NDA215910

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

12-25-2022

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

62756 - Sun Pharmaceutical Industries, Inc.
- 62756-301 - Sezaby
  - 62756-301-01 - 1 INJECTION in 1 VIAL, SINGLE-DOSE

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 62756-301-01?

The NDC Packaged Code 62756-301-01 is assigned to a package of 1 injection in 1 vial, single-dose of Sezaby, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is injection and is administered via intravenous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 62756-301 included in the NDC Directory?

Yes, Sezaby with product code 62756-301 is active and included in the NDC Directory. The product was first marketed by Sun Pharmaceutical Industries, Inc. on December 25, 2022 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 62756-301-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 62756-301-01?

The 11-digit format is 62756030101. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	62756-301-01	5-4-2	62756-0301-01

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