NDC codes

FDA NDC Directory
Product NDC (as listed)10135-799Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10135-0799Add 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
10135-799-601013507996060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-799-60)Marketed from Jul 1, 2025
10135-799-86101350799866 BLISTER PACK in 1 CARTON (10135-799-86) / 10 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jul 1, 2025

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 — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218014
Marketing start
Listing expires
DEA schedule
CV
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 10135-799_67afbd17-4406-4e18-a302-c0a5829ec903SPL ID 67afbd17-4406-4e18-a302-c0a5829ec903SPL set ID 0a273024-c2d2-4fae-90c3-b2f38a323f24RxCUI 809987, 809992, 809996, 810000UNII 563KS2PQY5UPC 0310135800605, 0310135799602, 0310135802609

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

N410135079960 followed by a unit qualifier and the quantity

Package 10135-0799-60. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 218014

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

FDA NDC Directory listings under ANDA 218014
ProductStrengthForm · routeLabelerProduct NDC
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc10135-800
LacosamideLacosamide 150 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc10135-801
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralMarlex Pharmaceuticals, Inc10135-802
LacosamideLacosamide 100 mg/1Tablet, Film coatedOralKanchan Healthcare Inc85742-009
LacosamideLacosamide 50 mg/1Tablet, Film coatedOralKanchan Healthcare Inc85742-008
LacosamideLacosamide 150 mg/1Tablet, Film coatedOralKanchan Healthcare Inc85742-010
LacosamideLacosamide 200 mg/1Tablet, Film coatedOralKanchan Healthcare Inc85742-011

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