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  5. NDC Package Code: 64679-730-01 Fosphenytoin Sodium

NDC Package 64679-730-01 Fosphenytoin Sodium

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 discontinued by the firm.

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:
64679-730-01
Package Description:
10 VIAL in 1 CARTON / 10 mL in 1 VIAL (64679-730-02)
Product Code:
64679-730
Proprietary Name:
Fosphenytoin Sodium
Usage Information:
Fosphenytoin sodium injection, USP is indicated for the treatment of generalized tonic-clonic status epilepticus and prevention and treatment of seizures occurring during neurosurgery. Fosphenytoin sodium injection, USP can also be substituted, short-term, for oral phenytoin. Fosphenytoin sodium injection, USP should be used only when oral phenytoin administration is not possible [see Dosage and Administration (2.4) and Warnings and Precautions (5.2)].
11-Digit NDC Billing Format:
64679073001
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
Labeler Name:
Wockhardt Usa Llc.
Sample Package:
No
FDA Application Number:
ANDA078137
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
08-06-2007
End Marketing Date:
07-01-2023
Listing Expiration Date:
07-01-2023
Exclude Flag:
D
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 64679-730-01?

The NDC Packaged Code 64679-730-01 is assigned to a package of 10 vial in 1 carton / 10 ml in 1 vial (64679-730-02) of Fosphenytoin Sodium, labeled by Wockhardt Usa Llc.. The product's dosage form is and is administered via form.

Is NDC 64679-730 included in the NDC Directory?

No, Fosphenytoin Sodium with product code 64679-730 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Wockhardt Usa Llc. on August 06, 2007 and its listing in the NDC Directory is set to expire on July 01, 2023 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 64679-730-01?

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 64679-730-01?

The 11-digit format is 64679073001. 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
5-3-264679-730-015-4-264679-0730-01