What is NDC 71921-223?

71921-223 is the product NDC for Lacosamide, Lacosamide 200 mg/1 tablet, listed with the FDA by Florida Pharmaceutical Products, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Lacosamide?

146 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lacosamide NDC 71921-223 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71921-223Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71921-0223Add 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 NDC	11-digit (billing)	Package	Copy
71921-223-06	7192102230671921022306	60 TABLET in 1 BOTTLE (71921-223-06)Marketed from Sep 21, 2023

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): Lacosamide
Generic name (nonproprietary): lacosamide
Active ingredients: Lacosamide — 200 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Florida Pharmaceutical Products, LLCNDC labeler code 71921
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208308
Marketing start: Sep 21, 2023
Listing expires: Dec 31, 2027
DEA schedule: CV
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 71921-223_85fd1828-d3d9-4b4b-965b-7ed7ef5f5e97SPL ID 85fd1828-d3d9-4b4b-965b-7ed7ef5f5e97SPL set ID 3680c0ff-7f5c-4572-b1eb-4fea96b7fbe2RxCUI 809987, 809992, 809996, 810000UNII 563KS2PQY5UPC 0371921221066, 0371921222063, 0371921223060

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

N471921022306 followed by a unit qualifier and the quantity

Package 71921-0223-06. 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 Feb 12, 2025.

Indications (excerpt from the label)

Lacosamide tablets are indicated for: Treatment of partial-onset seizures in patients 1 month of age and older (1.1) Adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients 4 years of age and older (1.2) 1.1 Partial-Onset Seizures Lacosamide tablets are indicated for the treatment of partial-onset seizures in patients 1 month of age and older. 1.2 Primary Generalized Tonic-Clonic Seizures Lacosamide tablets are indicated as adjunctive therapy in the treatment of primary generalized tonic-clonic seizures in patients 4 years of age and older.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71921-223

What is NDC 71921-223?: 71921-223 is the product NDC for Lacosamide, Lacosamide 200 mg/1 tablet, 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?: Lacosamide.
What is the active ingredient?: Lacosamide.
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 Lacosamide?: 146 other product NDCs are listed under this name. See all Lacosamide 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 Lacosamide NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lacosamide	Lacosamide 50 mg/1	TabletOral	AvPAK	50268-491	50268-0491-10
Lacosamide	Lacosamide 100 mg/1	TabletOral	AvPAK	50268-492	50268-0492-10
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4689	70518-4689-0070518-4689-0270518-4689-03
Lacosamide	Lacosamide 10 mg/mL	Injection, SolutionIntravenous	GLENMARK PHARMACEUTICALS INC., USA	68462-697	68462-0697-30
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4562	70518-4562-00
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4561	70518-4561-0070518-4561-02
Lacosamide	Lacosamide 10 mg/mL	Injection, SolutionIntravenous	Anthea Pharma Private Limited	83854-002	83854-0002-10
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4503	70518-4503-00
Lacosamide	Lacosamide 200 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4504	70518-4504-0070518-4504-0170518-4504-03
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4505	70518-4505-00

All 147 Lacosamide NDCs

Other NDCs under ANDA 208308

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

FDA NDC Directory listings under ANDA 208308
Product	Strength	Form · route	Labeler	Product NDC
Lacosamide	Lacosamide 50 mg/1	TabletOral	Indoco Remedies Limited	14445-129
Lacosamide	Lacosamide 100 mg/1	TabletOral	Indoco Remedies Limited	14445-130
Lacosamide	Lacosamide 150 mg/1	TabletOral	Indoco Remedies Limited	14445-131
Lacosamide	Lacosamide 200 mg/1	TabletOral	Indoco Remedies Limited	14445-132
Lacosamide	Lacosamide 50 mg/1	TabletOral	NorthStar RxLLC	16714-548
Lacosamide	Lacosamide 100 mg/1	TabletOral	NorthStar RxLLC	16714-549
Lacosamide	Lacosamide 150 mg/1	TabletOral	NorthStar RxLLC	16714-550
Lacosamide	Lacosamide 200 mg/1	TabletOral	NorthStar RxLLC	16714-552
Lacosamide	Lacosamide 50 mg/1	TabletOral	Tris Pharma Inc	27808-243
Lacosamide	Lacosamide 100 mg/1	TabletOral	Tris Pharma Inc	27808-244
Lacosamide	Lacosamide 150 mg/1	TabletOral	Tris Pharma Inc	27808-245
Lacosamide	Lacosamide 200 mg/1	TabletOral	Tris Pharma Inc	27808-246
Lacosamide	Lacosamide 50 mg/1	TabletOral	AvPAK	50268-491
Lacosamide	Lacosamide 100 mg/1	TabletOral	AvPAK	50268-492
Lacosamide	Lacosamide 50 mg/1	TabletOral	Florida Pharmaceutical Products, LLC	71921-220
Lacosamide	Lacosamide 100 mg/1	TabletOral	Florida Pharmaceutical Products, LLC	71921-221
Lacosamide	Lacosamide 150 mg/1	TabletOral	Florida Pharmaceutical Products, LLC	71921-222