What is NDC 70518-4504?

70518-4504 is the product NDC for Lacosamide, Lacosamide 200 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-4504 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4504Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4504Add 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
70518-4504-0	70518450400	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4504-0)Marketed from Oct 14, 2025
70518-4504-1	70518450401	30 POUCH in 1 BOX (70518-4504-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-4504-2)Marketed from Feb 2, 2026
70518-4504-3	70518450403	50 POUCH in 1 BOX (70518-4504-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-4504-2)Marketed from Jul 20, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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, Film coated
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 204974
Marketing start: Oct 14, 2025
Listing expires: Dec 31, 2027
DEA schedule: CV
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 70518-4504_571e0769-5636-4926-e063-6394a90a8d7aSPL ID 571e0769-5636-4926-e063-6394a90a8d7aSPL set ID edd20b60-6265-4c4e-a95a-aaf8103cd852RxCUI 809996UNII 563KS2PQY5

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

N470518450400 followed by a unit qualifier and the quantity

Package 70518-4504-00. 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 Jul 21, 2026.

Indications (excerpt from the label)

Lacosamide tablets are indicated for: • Treatment of partial-onset seizures in patients 4 years 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 4 years of age and older. Additional pediatric use information is approved for UCB, Inc.’s VIMPAT ® (lacosamide) tablets. However, due to UCB, Inc.’s marketing exclusivity rights, this drug product is not labeled with that information. 1.2 Primary Generalized Tonic-Clonic Seizures Lacosamide tablets are indicated as adjunctive therapy in…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4504

What is NDC 70518-4504?: 70518-4504 is the product NDC for Lacosamide, Lacosamide 200 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 3 package NDCs, 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?: REMEDYREPACK INC., NDC labeler code 70518. 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.	70518-4561	70518-4561-0070518-4561-02
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4562	70518-4562-00
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 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4505	70518-4505-00
Lacosamide	Lacosamide 50 mg/5mL	SolutionOral	Precision Dose, Inc.	68094-076	68094-0076-62

All 147 Lacosamide NDCs

Other NDCs under ANDA 204974

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

FDA NDC Directory listings under ANDA 204974
Product	Strength	Form · route	Labeler	Product NDC
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-171
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-172
Lacosamide	Lacosamide 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-173
Lacosamide	Lacosamide 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Limited	46708-174
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-171
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-172
Lacosamide	Lacosamide 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-173
Lacosamide	Lacosamide 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-174
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4503
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4505