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  5. NDC Package Code: 65162-065-87 Sodium Oxybate

NDC Package 65162-065-87 Sodium Oxybate

Solution Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
65162-065-87
Package Description:
1 BOTTLE in 1 CARTON / 180 mL in 1 BOTTLE
Product Code:
65162-065
Proprietary Name:
Sodium Oxybate
Non-Proprietary Name:
Sodium Oxybate
Substance Name:
Sodium Oxybate
Usage Information:
This medication is used to treat narcolepsy, a condition that causes severe daytime sleepiness. Sodium oxybate can decrease daytime sleepiness and also reduce the number of sudden short attacks of weak/paralyzed muscles (known as cataplexy) that can occur in patients with narcolepsy. Sodium oxybate is a central nervous system depressant. It is also known as gamma hydroxybutyrate (GHB).
11-Digit NDC Billing Format:
65162006587
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Amneal Pharmaceuticals Llc
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
SODIUM OXYBATE 500 mg/mL
Pharmacologic Class(es):
DEA Schedule:
Schedule III (CIII) Substances
Sample Package:
No
FDA Application Number:
ANDA203631
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
09-12-2025
Listing Expiration Date:
12-31-2026
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.

Frequently Asked Questions

What is NDC 65162-065-87?

The NDC Packaged Code 65162-065-87 is assigned to a package of 1 bottle in 1 carton / 180 ml in 1 bottle of Sodium Oxybate, a human prescription drug labeled by Amneal Pharmaceuticals Llc. The product's dosage form is solution and is administered via oral form.

Is NDC 65162-065 included in the NDC Directory?

Yes, Sodium Oxybate with product code 65162-065 is active and included in the NDC Directory. The product was first marketed by Amneal Pharmaceuticals Llc on September 12, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 65162-065-87?

The 11-digit format is 65162006587. 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
5-3-265162-065-875-4-265162-0065-87