NDC codes

FDA NDC Directory
Product NDC (as listed)67046-0749Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67046-0749Add 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
67046-0749-36704607490330 TABLET in 1 BLISTER PACK (67046-0749-3)Marketed from Jun 16, 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)
Lamotrigine
Generic name (nonproprietary)
lamotrigine
Active ingredients
Lamotrigine — 150 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 090170
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)Dihydrofolate Reductase Inhibitors (Mechanism)Organic Cation Transporter 2 Inhibitors (Mechanism)
Identifiers
Product ID 67046-0749_545fcb8e-1f7a-c2f7-e063-6394a90a004dSPL ID 545fcb8e-1f7a-c2f7-e063-6394a90a004dSPL set ID 545fcc0e-1e2b-bdcb-e063-6294a90a4ac7RxCUI 198428UNII U3H27498KS
Pharmacologic class
Anti-epileptic Agent; Mood Stabilizer

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

N467046074903 followed by a unit qualifier and the quantity

Package 67046-0749-03. 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 090170

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

FDA NDC Directory listings under ANDA 090170
ProductStrengthForm · routeLabelerProduct NDC
LamotrigineLamotrigine 100 mg/1TabletOralCoupler LLC67046-0359
LamotrigineLamotrigine 150 mg/1TabletOralREMEDYREPACK INC.70518-1978
LamotrigineLamotrigine 200 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-114
LamotrigineLamotrigine 25 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-111
LamotrigineLamotrigine 100 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-112
LamotrigineLamotrigine 150 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-113
LamotrigineLamotrigine 25 mg/1TabletOralCoupler LLC67046-0358
LamotrigineLamotrigine 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7223
LamotrigineLamotrigine 100 mg/1TabletOralREMEDYREPACK INC.70518-2343
LamotrigineLamotrigine 150 mg/1TabletOralA-S Medication Solutions50090-2131
LamotrigineLamotrigine 25 mg/1TabletOralA-S Medication Solutions50090-2129
LamotrigineLamotrigine 100 mg/1TabletOralA-S Medication Solutions50090-2130
LamotrigineLamotrigine 150 mg/1TabletOralBryant Ranch Prepack71335-1110
LamotrigineLamotrigine 25 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7544
LamotrigineLamotrigine 200 mg/1TabletOralREMEDYREPACK INC.70518-2406
LamotrigineLamotrigine 25 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-0289
LamotrigineLamotrigine 25 mg/1TabletOralNorthwind Health Company, LLC51655-719
LamotrigineLamotrigine 200 mg/1TabletOralREMEDYREPACK INC.70518-1479
LamotrigineLamotrigine 25 mg/1TabletOralBryant Ranch Prepack71335-1179
LamotrigineLamotrigine 150 mg/1TabletOralREMEDYREPACK INC.70518-2577

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