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  5. NDC Package Code: 0641-0476-25 Phenobarbital Sodium

NDC Package 0641-0476-25 Phenobarbital Sodium

Injection Intramuscular; Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. 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:
0641-0476-25
Package Description:
25 VIAL in 1 CARTON / 1 mL in 1 VIAL (0641-0476-21)
Product Code:
0641-0476
Proprietary Name:
Phenobarbital Sodium
Non-Proprietary Name:
Phenobarbital Sodium
Substance Name:
Phenobarbital Sodium
Usage Information:
Barbiturates are contraindicated in patients with known barbiturate sensitivity. Barbiturates are also contraindicated in patients with a history of manifest or latent porphyria, marked impairment of liver functions or with severe respiratory distress where dyspnea or obstruction is evident. Large doses are contraindicated in nephritic subjects.Barbiturates should not be administered to persons with known previous addiction to the sedative-hypnotic group since ordinary doses may be ineffectual and may contribute to further addiction.Intraarterial administration is contraindicated. Its consequences vary from transient pain to gangrene. Subcutaneous administration produces tissue irritation, ranging from tenderness and redness to necrosis and is not recommended. (See DOSAGE AND ADMINISTRATION, Treatment of Adverse Effects Due to Inadvertent Error in Administration.)
11-Digit NDC Billing Format:
00641047625
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 198368 - PHENobarbital 65 MG/ML Injectable Solution
  • RxCUI: 198368 - phenobarbital 65 MG/ML Injectable Solution
  • RxCUI: 312370 - PHENobarbital 130 MG/ML Injectable Solution
  • RxCUI: 312370 - phenobarbital 130 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Hikma Pharmaceuticals Usa 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):
  • Intramuscular - Administration within a muscle.
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • PHENOBARBITAL SODIUM 65 mg/mL
    • DEA Schedule:
    Schedule IV (CIV) Substances
    Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    01-01-1971
    Listing Expiration Date:
    12-31-2025
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 0641-0476-25 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    00641047625J2560Phenobarbital sodium inj120 MG1250.5413.5

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0641-0476-25?

    The NDC Packaged Code 0641-0476-25 is assigned to a package of 25 vial in 1 carton / 1 ml in 1 vial (0641-0476-21) of Phenobarbital Sodium, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection and is administered via intramuscular; intravenous form.

    Is NDC 0641-0476 included in the NDC Directory?

    Yes, Phenobarbital Sodium with product code 0641-0476 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on January 01, 1971 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0641-0476-25?

    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 0641-0476-25?

    The 11-digit format is 00641047625. 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 4-4-2 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
    4-4-20641-0476-255-4-200641-0476-25