What is NDC 59746-247?

59746-247 is the product NDC for Lamotrigine, Lamotrigine 150 mg/1 tablet, listed with the FDA by Jubilant Cadista Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

Jubilant Cadista Pharmaceuticals Inc., NDC labeler code 59746. 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?

262 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lamotrigine NDC 59746-247 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)59746-247Labeler and product segments. Claims need a package NDC.

Product NDC at billing width59746-0247Add 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
59746-247-05	5974602470559746024705	500 TABLET in 1 BOTTLE (59746-247-05)Marketed from Jan 27, 2009
59746-247-60	5974602476059746024760	60 TABLET in 1 BOTTLE (59746-247-60)Marketed from Jan 27, 2009
59746-247-90	5974602479059746024790	90 TABLET in 1 BOTTLE (59746-247-90)Marketed from Jan 27, 2009

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 — 150 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Jubilant Cadista Pharmaceuticals Inc.NDC labeler code 59746
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 079132
Marketing start: Jan 27, 2009
Listing expires: Dec 31, 2027
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 59746-247_a8edaf38-c040-4080-91ec-fc456a9ecde6SPL ID a8edaf38-c040-4080-91ec-fc456a9ecde6
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

N459746024705 followed by a unit qualifier and the quantity

Package 59746-0247-05. 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 59746-247

What is NDC 59746-247?: 59746-247 is the product NDC for Lamotrigine, Lamotrigine 150 mg/1 tablet, listed with the FDA by Jubilant Cadista Pharmaceuticals Inc.. It has 3 package NDCs, 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?: Jubilant Cadista Pharmaceuticals Inc., NDC labeler code 59746. 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?: 262 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lamotrigine	Lamotrigine 50 mg/1	Tablet, Extended releaseOral	REMEDYREPACK INC.	70518-4702	70518-4702-00
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	Coupler LLC	67046-0358	67046-0358-03
Lamotrigine	Lamotrigine 150 mg/1	TabletOral	Coupler LLC	67046-0749	67046-0749-03
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	Coupler LLC	67046-0359	67046-0359-03
lamotriginelamotrigine extended-release	Lamotrigine 200 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-4638	70518-4638-00
Lamotrigine	Lamotrigine 25 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Inc.	62332-770	62332-0770-1562332-0770-30
Lamotrigine	Lamotrigine 50 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Inc.	62332-771	62332-0771-1562332-0771-30
Lamotrigine	Lamotrigine 100 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Inc.	62332-772	62332-0772-1062332-0772-30
Lamotrigine	Lamotrigine 200 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Inc.	62332-773	62332-0773-1062332-0773-30
Lamotrigine	Lamotrigine 25 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Limited	46708-770	46708-0770-1546708-0770-30

All 263 Lamotrigine NDCs

Other NDCs under ANDA 079132

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

FDA NDC Directory listings under ANDA 079132
Product	Strength	Form · route	Labeler	Product NDC
Lamotrigine	Lamotrigine 200 mg/1	TabletOral	AvKARE	42291-369
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	AvKARE	42291-366
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	AvKARE	42291-367
Lamotrigine	Lamotrigine 150 mg/1	TabletOral	AvKARE	42291-368
Lamotrigine	Lamotrigine 150 mg/1	TabletOral	Bryant Ranch Prepack	63629-4697
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	Jubilant Cadista Pharmaceuticals Inc.	59746-245
Lamotrigine	Lamotrigine 200 mg/1	TabletOral	Jubilant Cadista Pharmaceuticals Inc.	59746-248
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	Jubilant Cadista Pharmaceuticals Inc.	59746-246