NDC codes

FDA NDC Directory
Product NDC (as listed)76282-822Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76282-0822Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
76282-822-60762820822607628208226060 TABLET, FILM COATED in 1 BOTTLE (76282-822-60)Marketed from Jul 28, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Brivaracetam
Generic name (nonproprietary)
brivaracetam
Active ingredients
Brivaracetam — 10 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Exelan Pharmaceuticals, IncNDC labeler code 76282
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 219952
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Epoxide Hydrolase Inhibitors (Mechanism)
Identifiers
Product ID 76282-822_a72c2804-469d-4405-b2b2-1d0ea7c9a7e3SPL ID a72c2804-469d-4405-b2b2-1d0ea7c9a7e3

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N476282082260 followed by a unit qualifier and the quantity

Package 76282-0822-60. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

The FDA listing for this product does not reference a label (SPL) set.

About NDC 76282-822

What is NDC 76282-822?
76282-822 is the product NDC for Brivaracetam, Brivaracetam 10 mg/1 tablet, film coated, listed with the FDA by Exelan Pharmaceuticals, Inc. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Brivaracetam.
What is the active ingredient?
Brivaracetam.
Who is the labeler?
Exelan Pharmaceuticals, Inc, NDC labeler code 76282. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Brivaracetam?
52 other product NDCs are listed under this name. See all Brivaracetam NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Brivaracetam NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BrivaracetamBrivaracetam 10 mg/mLSolutionOralAurobindo Pharma Limited59651-99559651-0995-03
BrivaracetamBrivaracetam 25 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-82376282-0823-60
BrivaracetamBrivaracetam 50 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-82476282-0824-60
BrivaracetamBrivaracetam 75 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-82576282-0825-60
BrivaracetamBrivaracetam 100 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-82676282-0826-60
BrivaracetamBrivaracetam 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-06884386-0068-60
BrivaracetamBrivaracetam 25 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-06984386-0069-60
BrivaracetamBrivaracetam 75 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-07184386-0071-60
brivaracetamBrivaracetam 25 mg/1Tablet, Film coatedOralAvKARE73190-07473190-0074-60
brivaracetamBrivaracetam 50 mg/1Tablet, Film coatedOralAvKARE73190-07573190-0075-60

All 53 Brivaracetam NDCs

Other NDCs under ANDA 219952

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 219952
ProductStrengthForm · routeLabelerProduct NDC
brivaracetamBrivaracetam 10 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-556
brivaracetamBrivaracetam 25 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-557
brivaracetamBrivaracetam 50 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-558
brivaracetamBrivaracetam 75 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-559
brivaracetamBrivaracetam 100 mg/1Tablet, Film coatedOralScieGen Pharmaceuticals, Inc.50228-560
BrivaracetamBrivaracetam 25 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-823
BrivaracetamBrivaracetam 50 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-824
BrivaracetamBrivaracetam 75 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-825
BrivaracetamBrivaracetam 100 mg/1Tablet, Film coatedOralExelan Pharmaceuticals, Inc76282-826

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