Prescription drug · ANDA

Lacosamide NDC 70518-4689

Lacosamide 50 mg/1 · Tablet, Film coated · Oral · REMEDYREPACK INC.

NDC codes

FDA NDC Directory
Product NDC (as listed)70518-4689Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-4689Add 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
70518-4689-0705184689007051846890030 POUCH in 1 BOX (70518-4689-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Marketed from Jul 3, 2026
70518-4689-27051846890270518468902100 POUCH in 1 BOX (70518-4689-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Marketed from Jul 6, 2026
70518-4689-3705184689037051846890350 POUCH in 1 BOX (70518-4689-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-4689-1)Marketed from Sep 23, 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 — 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 214695
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 70518-4689_5c266de9-61e6-107b-e063-6394a90af427SPL ID 5c266de9-61e6-107b-e063-6394a90af427

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

N470518468900 followed by a unit qualifier and the quantity

Package 70518-4689-00. 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 70518-4689

What is NDC 70518-4689?
70518-4689 is the product NDC for Lacosamide, Lacosamide 50 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LacosamideLacosamide 50 mg/1TabletOralAvPAK50268-49150268-0491-10
LacosamideLacosamide 100 mg/1TabletOralAvPAK50268-49250268-0492-10
LacosamideLacosamide 10 mg/mLInjection, SolutionIntravenousGLENMARK PHARMACEUTICALS INC., USA68462-69768462-0697-30
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-456270518-4562-00
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-456170518-4561-0070518-4561-02
LacosamideLacosamide 10 mg/mLInjection, SolutionIntravenousAnthea Pharma Private Limited83854-00283854-0002-10
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-450370518-4503-00
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-450470518-4504-0070518-4504-0170518-4504-03
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-450570518-4505-00
LacosamideLacosamide 50 mg/5mLSolutionOralPrecision Dose, Inc.68094-07668094-0076-62

All 147 Lacosamide NDCs

Other NDCs under ANDA 214695

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

FDA NDC Directory listings under ANDA 214695
ProductStrengthForm · routeLabelerProduct NDC
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7244
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7245
LacosamideLacosamide 150 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7246
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-7247
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-676
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-687
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-698
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-733
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-734
LacosamideLacosamide 150 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-735
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralAscend Laboratories, LLC67877-736
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-4561
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralAdvanced Rx of Tennessee, LLC80425-0510

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