Lamotrigine NDC 27241-186

NDC codes

FDA NDC Directory

Product NDC (as listed)27241-186Labeler and product segments. Claims need a package NDC.

Product NDC at billing width27241-0186Add 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
27241-186-30	27241018630	30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (27241-186-30)Marketed from Jan 19, 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 — 200 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: Ajanta Pharma USA Inc.
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 213271
Marketing start: Jan 19, 2021
Listing expires: Dec 31, 2026
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 27241-186_9791ac5c-7be4-4ff8-8de3-21ab21346ca9SPL ID 9791ac5c-7be4-4ff8-8de3-21ab21346ca9SPL set ID 9dfb5f87-0150-4c26-a89f-34f1ab389500RxCUI 103968, 198430, 252478, 252479UNII U3H27498KSUPC 0327241184307, 0327241186301, 0327241183300, 0327241185304
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

N427241018630 followed by a unit qualifier and the quantity

Package 27241-0186-30. 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

Current FDA label (SPL), effective Nov 26, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Lamotrigine orally disintegrating tablets are indicated for: Epilepsy—adjunctive therapy in patients aged 2 years and older: partial-onset seizures. primary generalized tonic-clonic (PGTC) seizures. generalized seizures of Lennox-Gastaut syndrome. ( 1.1 ) Epilepsy—monotherapy in patients aged 16 years and older: Conversion to monotherapy in patients with partial-onset seizures who are receiving treatment with carbamazepine, phenytoin, phenobarbital, primidone, or valproate as the single antiepileptic drug. ( 1.1 ) Bipolar disorder: Maintenance treatment of bipolar I disorder to delay the time to occurrence of mood episodes in patients treated for acute mood episodes with standard therapy. ( …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 213271

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

FDA NDC Directory listings under ANDA 213271
Product	Strength	Form · route	Labeler	Product NDC
Lamotrigine	Lamotrigine 100 mg/1	Tablet, Orally disintegratingOral	Ajanta Pharma USA Inc.	27241-185
Lamotrigine	Lamotrigine 25 mg/1	Tablet, Orally disintegratingOral	Ajanta Pharma USA Inc.	27241-183
Lamotrigine	Lamotrigine 50 mg/1	Tablet, Orally disintegratingOral	Ajanta Pharma USA Inc.	27241-184