Elepsia Xr 1500 Mg Tablet, Extended Release
NDC Package 80705-101-30

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Elepsia Xr 1500 Mg (levetiracetam) tablets is levetiracetam is used to treat seizures (epilepsy). This formulation utilizes a tablet, extended release delivery system. Marketed by Tripoint Therapeutics, Llc, this product is identified by NDC 80705-101 and is authorized under FDA application NDA204417.

Identification & Billing

NDC Package Code
80705-101-30
Package Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Code
11-Digit Billing Format
80705010130
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
30 EA
RxNorm Crosswalk
  • RxCUI: 1605362 - levETIRAcetam 1000 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1605362 - 24 HR levetiracetam 1000 MG Extended Release Oral Tablet
  • RxCUI: 1605362 - levetiracetam 1000 MG 24 HR Extended Release Oral Tablet
  • RxCUI: 1605368 - Elepsia XR 1000 MG 24HR Extended Release Oral Tablet
  • RxCUI: 1605368 - 24 HR levetiracetam 1000 MG Extended Release Oral Tablet [Elepsia]

Clinical Specifications

Proprietary Name
Elepsia Xr 1500 Mg
Non-Proprietary Name
Levetiracetam
Substance Name
Levetiracetam
Dosage Form
Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Levetiracetam is used to treat seizures (epilepsy). It belongs to a class of drugs known as anticonvulsants. Levetiracetam may decrease the number of seizures you have.

Regulatory & Marketing

Labeler Name
Tripoint Therapeutics, Llc
Product Type
Human Prescription Drug
FDA Application #
NDA204417
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
02-12-2021
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (80705-101). Click a package code to view its specific billing and regulatory data.

1 BLISTER PACK in 1 CARTON / 2 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
1 BLISTER PACK in 1 CARTON / 7 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 80705-101-30 identifies a specific commercial package of 30 tablet, extended release in 1 bottle, plastic of Elepsia Xr 1500 Mg, a human prescription drug labeled by Tripoint Therapeutics, Llc. This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package. This tablet, extended release is formulated for oral use and contains levetiracetam as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Tripoint Therapeutics, Llc on February 12, 2021. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Levetiracetam is used to treat seizures (epilepsy). It belongs to a class of drugs known as anticonvulsants. Levetiracetam may decrease the number of seizures you have.

How is this Tripoint Therapeutics, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 80705010130. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 30 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
80705-101-30
11-Digit CMS (5-4-2)
80705-0101-30

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.