What is NDC 70518-4503?

70518-4503 is the product NDC for Lacosamide, Lacosamide 50 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, 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?

144 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 70518-4503 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4503Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4503Add 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
70518-4503-0	70518450300	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4503-0)Marketed from Oct 14, 2025

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 — 50 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 70518-4503_5b862910-fd83-9666-e063-6294a90a2539SPL ID 5b862910-fd83-9666-e063-6294a90a2539

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

N470518450300 followed by a unit qualifier and the quantity

Package 70518-4503-00. 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

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

About NDC 70518-4503

What is NDC 70518-4503?: 70518-4503 is the product NDC for Lacosamide, Lacosamide 50 mg/1 tablet, film coated, listed with the FDA by REMEDYREPACK INC.. 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?: 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?: 144 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	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 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
Lacosamide	Lacosamide 100 mg/10mL	SolutionOral	Precision Dose, Inc.	68094-176	68094-0176-62
Lacosamide	Lacosamide 50 mg/5mL	SolutionOral	Precision Dose, Inc.	68094-076	68094-0076-62
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	Kanchan Healthcare Inc	85742-008	85742-0008-0785742-0008-08

All 145 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 200 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-174
Lacosamide	Lacosamide 50 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-171
Lacosamide	Lacosamide 200 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4504
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-172
Lacosamide	Lacosamide 100 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-4505
Lacosamide	Lacosamide 150 mg/1	Tablet, Film coatedOral	Alembic Pharmaceuticals Inc.	62332-173