NDC codes

FDA NDC Directory
Product NDC (as listed)71921-410Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71921-0410Add 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
71921-410-72719210410721 BOTTLE in 1 CARTON (71921-410-72) / 300 mL in 1 BOTTLEMarketed from Feb 24, 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 oral Solution
Generic name (nonproprietary)
brivaracetam oral
Active ingredients
Brivaracetam — 10 mg/mL
Dosage form
Solution
Route
Oral
Labeler
Florida Pharmaceutical Products, LLCNDC labeler code 71921
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 220385
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Epoxide Hydrolase Inhibitors (Mechanism)
Identifiers
Product ID 71921-410_7957cc22-2e0f-489d-9fa1-99520f615934SPL ID 7957cc22-2e0f-489d-9fa1-99520f615934SPL set ID 7957cc22-2e0f-489d-9fa1-99520f615934RxCUI 1739785UNII U863JGG2IAUPC 0371921410729

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

N471921041072 followed by a unit qualifier and the quantity

Package 71921-0410-72. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Brivaracetam oral solution is indicated for the treatment of partial-onset seizures in patients 1 month of age and older. Brivaracetam oral solution is indicated for the treatment of partial-onset seizures in patients 1 month of age and older. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71921-410

What is NDC 71921-410?
71921-410 is the product NDC for Brivaracetam oral Solution (brivaracetam oral), Brivaracetam 10 mg/mL solution, listed with the FDA by Florida Pharmaceutical Products, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Brivaracetam oral Solution (Brivaracetam oral).
What is the active ingredient?
Brivaracetam.
Who is the labeler?
Florida Pharmaceutical Products, LLC, NDC labeler code 71921. 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 oral Solution?
1 other product NDC are listed under this name. See all Brivaracetam oral Solution 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 oral Solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Brivaracetam Oral SolutionbrivaracetamBrivaracetam 10 mg/mLSolutionOralAscend Laboratories, LLC67877-90467877-0904-58

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