NDC codes

FDA NDC Directory
Product NDC (as listed)72789-206Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0206Add 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
72789-206-607278902066060 TABLET in 1 BOTTLE, PLASTIC (72789-206-60)Marketed from Sep 27, 2021

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)
Lamotrigine
Generic name (nonproprietary)
lamotrigine
Active ingredients
Lamotrigine — 100 mg/1
Dosage form
Tablet
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 72789
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 72789-206_5b73e90b-d594-70c2-e063-6394a90ac8f9SPL ID 5b73e90b-d594-70c2-e063-6394a90ac8f9
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

N472789020660 followed by a unit qualifier and the quantity

Package 72789-0206-60. 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

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

About NDC 72789-206

What is NDC 72789-206?
72789-206 is the product NDC for Lamotrigine, Lamotrigine 100 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lamotrigine.
What is the active ingredient?
Lamotrigine.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 72789. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lamotrigine?
259 other product NDCs are listed under this name. See all Lamotrigine 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 Lamotrigine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LamotrigineLamotrigine 50 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-470270518-4702-00
LamotrigineLamotrigine 25 mg/1TabletOralCoupler LLC67046-035867046-0358-03
LamotrigineLamotrigine 150 mg/1TabletOralCoupler LLC67046-074967046-0749-03
LamotrigineLamotrigine 100 mg/1TabletOralCoupler LLC67046-035967046-0359-03
lamotriginelamotrigine extended-releaseLamotrigine 200 mg/1Tablet, Film coated, Extended releaseOralREMEDYREPACK INC.70518-463870518-4638-00
LamotrigineLamotrigine 25 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-77046708-0770-1546708-0770-30
LamotrigineLamotrigine 50 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-77146708-0771-1546708-0771-30
LamotrigineLamotrigine 100 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-77246708-0772-1046708-0772-30
LamotrigineLamotrigine 200 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Limited46708-77346708-0773-1046708-0773-30
LamotrigineLamotrigine 25 mg/1Tablet, Orally disintegratingOralAlembic Pharmaceuticals Inc.62332-77062332-0770-1562332-0770-30

All 260 Lamotrigine NDCs

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 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 200 mg/1TabletOralUnichem Pharmaceuticals (USA), Inc.29300-114
LamotrigineLamotrigine 25 mg/1TabletOralA-S Medication Solutions50090-2129
LamotrigineLamotrigine 100 mg/1TabletOralA-S Medication Solutions50090-2130
LamotrigineLamotrigine 150 mg/1TabletOralA-S Medication Solutions50090-2131
LamotrigineLamotrigine 200 mg/1TabletOralA-S Medication Solutions50090-3914
LamotrigineLamotrigine 25 mg/1TabletOralNorthwind Health Company, LLC51655-719
LamotrigineLamotrigine 25 mg/1TabletOralProficient Rx LP63187-487
LamotrigineLamotrigine 25 mg/1TabletOralCoupler LLC67046-0358
LamotrigineLamotrigine 100 mg/1TabletOralCoupler LLC67046-0359
LamotrigineLamotrigine 150 mg/1TabletOralCoupler LLC67046-0749
LamotrigineLamotrigine 100 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-7223
LamotrigineLamotrigine 25 mg/1TabletOralPreferred Pharmaceuticals, Inc.68788-7544
LamotrigineLamotrigine 200 mg/1TabletOralREMEDYREPACK INC.70518-1479
LamotrigineLamotrigine 25 mg/1TabletOralREMEDYREPACK INC.70518-1908
LamotrigineLamotrigine 150 mg/1TabletOralREMEDYREPACK INC.70518-1978
LamotrigineLamotrigine 100 mg/1TabletOralREMEDYREPACK INC.70518-2343
LamotrigineLamotrigine 200 mg/1TabletOralREMEDYREPACK INC.70518-2406

Showing 20 of 30.

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