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  5. NDC Package Code: 0121-4067-40 Gabapentin

NDC Package 0121-4067-40 Gabapentin

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:
0121-4067-40
Package Description:
4 TRAY in 1 CASE / 10 CUP, UNIT-DOSE in 1 TRAY / 5 mL in 1 CUP, UNIT-DOSE (0121-4067-05)
Product Code:
0121-4067
Proprietary Name:
Gabapentin
Non-Proprietary Name:
Gabapentin
Substance Name:
Gabapentin
Usage Information:
Gabapentin is used with other medications to prevent and control seizures. It is also used to relieve nerve pain following shingles (a painful rash due to herpes zoster infection) in adults. Gabapentin is known as an anticonvulsant or antiepileptic drug.
11-Digit NDC Billing Format:
00121406740
Product Type:
Human Prescription Drug
Labeler Name:
Pai Holdings, Llc Dba Pai Pharma
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):
GABAPENTIN 250 mg/5mL
Pharmacologic Class(es):
Decreased Central Nervous System Disorganized Electrical Activity - [PE] (Physiologic Effect)
Sample Package:
No
FDA Application Number:
ANDA211330
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
06-12-2025
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 0121-4067-40?

The NDC Packaged Code 0121-4067-40 is assigned to a package of 4 tray in 1 case / 10 cup, unit-dose in 1 tray / 5 ml in 1 cup, unit-dose (0121-4067-05) of Gabapentin, a human prescription drug labeled by Pai Holdings, Llc Dba Pai Pharma. The product's dosage form is solution and is administered via oral form.

Is NDC 0121-4067 included in the NDC Directory?

Yes, Gabapentin with product code 0121-4067 is active and included in the NDC Directory. The product was first marketed by Pai Holdings, Llc Dba Pai Pharma on June 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 0121-4067-40?

The 11-digit format is 00121406740. 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
4-4-20121-4067-405-4-200121-4067-40