What is NDC 43063-203?

43063-203 is the product NDC for Lamotrigine, Lamotrigine 100 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lamotrigine NDC 43063-203 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43063-203Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43063-0203Add 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
43063-203-30	43063020330	30 TABLET in 1 BOTTLE, PLASTIC (43063-203-30)Marketed from Aug 13, 2010
43063-203-60	43063020360	60 TABLET in 1 BOTTLE, PLASTIC (43063-203-60)Marketed from Aug 13, 2010
43063-203-90	43063020390	90 TABLET in 1 BOTTLE, PLASTIC (43063-203-90)Marketed from Aug 13, 2010

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 43063
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078947
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 43063-203_5c187fbb-619c-17f5-e063-6294a90ab01dSPL ID 5c187fbb-619c-17f5-e063-6294a90ab01d
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

N443063020330 followed by a unit qualifier and the quantity

Package 43063-0203-30. 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

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

About NDC 43063-203

What is NDC 43063-203?: 43063-203 is the product NDC for Lamotrigine, Lamotrigine 100 mg/1 tablet, listed with the FDA by PD-Rx 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?: PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. 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
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 Limited	46708-770	46708-0770-1546708-0770-30
Lamotrigine	Lamotrigine 50 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Limited	46708-771	46708-0771-1546708-0771-30
Lamotrigine	Lamotrigine 100 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Limited	46708-772	46708-0772-1046708-0772-30
Lamotrigine	Lamotrigine 200 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Limited	46708-773	46708-0773-1046708-0773-30
Lamotrigine	Lamotrigine 25 mg/1	Tablet, Orally disintegratingOral	Alembic Pharmaceuticals Inc.	62332-770	62332-0770-1562332-0770-30

All 260 Lamotrigine NDCs

Other NDCs under ANDA 078947

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

FDA NDC Directory listings under ANDA 078947
Product	Strength	Form · route	Labeler	Product NDC
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-047
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-045
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	Northwind Health Company, LLC	51655-855
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	OWP Pharmaceuticals, Inc.	69102-639
Lamotrigine	—	Kit	Torrent Pharmaceuticals Limited	13668-266
Lamotrigine	Lamotrigine 200 mg/1	TabletOral	A-S Medication Solutions	50090-6028
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-238
Lamotrigine	Lamotrigine 150 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-048
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3607
Lamotrigine	Lamotrigine 200 mg/1	TabletOral	Torrent Pharmaceuticals Limited	13668-049
Lamotrigine	Lamotrigine 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-2755
Lamotrigine	Lamotrigine 100 mg/1	TabletOral	REMEDYREPACK INC.	70518-2889
LAMOTRIGINE Kitlamotrigine	—	Kit	OWP Pharmaceuticals, Inc.	69102-137
Subvenitelamotrigine	Lamotrigine 150 mg/1	TabletOral	OWP Pharmaceuticals, Inc.	69102-150
Subvenitelamotrigine	—	Kit	OWP Pharmaceuticals, Inc.	69102-312
Subvenitelamotrigine	—	Kit	OWP Pharmaceuticals, Inc.	69102-300
Subvenitelamotrigine	Lamotrigine 25 mg/1	TabletOral	OWP Pharmaceuticals, Inc.	69102-301
Subvenitelamotrigine	—	Kit	OWP Pharmaceuticals, Inc.	69102-306
Subvenitelamotrigine	Lamotrigine 100 mg/1	TabletOral	OWP Pharmaceuticals, Inc.	69102-319
Subvenitelamotrigine	Lamotrigine 200 mg/1	TabletOral	OWP Pharmaceuticals, Inc.	69102-320

Showing 20 of 21.