What is NDC 68001-404?

68001-404 is the product NDC for Levetiracetam, Levetiracetam 750 mg/1 tablet, film coated, listed with the FDA by BluePoint Laboratories. It has 2 package NDCs, shown above in 10- and 11-digit form.

BluePoint Laboratories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Levetiracetam?

260 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Levetiracetam NDC 68001-404 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68001-404Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68001-0404Add 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
68001-404-03	6800104040368001040403	500 TABLET, FILM COATED in 1 BOTTLE (68001-404-03)Marketed from Jun 19, 2019
68001-404-07	6800104040768001040407	120 TABLET, FILM COATED in 1 BOTTLE (68001-404-07)Marketed from Jun 19, 2019

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): Levetiracetam
Generic name (nonproprietary): levetiracetam
Active ingredients: Levetiracetam — 750 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: BluePoint LaboratoriesNDC labeler code 68001
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078993
Marketing start: Jun 19, 2019
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 68001-404_28d8b606-37b2-642c-e063-6294a90ad080SPL ID 28d8b606-37b2-642c-e063-6294a90ad080SPL set ID 8b74b8bc-d95c-4471-8f74-c3117243bf89RxCUI 311288, 311289, 311290, 387003UNII 44YRR34555

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

N468001040403 followed by a unit qualifier and the quantity

Package 68001-0404-03. 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

Current FDA label (SPL), effective Dec 11, 2024.

Indications (excerpt from the label)

Levetiracetam is indicated for the treatment of partial-onset seizures in patients 1 month of age and older ( 1.1 ) Levetiracetam is indicated for adjunctive therapy for the treatment of: Myoclonic seizures in patients 12 years of age and older with juvenile myoclonic epilepsy (1.2) Primary generalized tonic-clonic seizures in patients 6 years of age and older with idiopathic generalized epilepsy (1.3) 1.1 Partial-Onset Seizures Levetiracetam tablets are indicated for the treatment of partial-onset seizures in patients 1 month of age and older. 1.2 Myoclonic Seizures in Patients with Juvenile Myoclonic Epilepsy Levetiracetam tablets are indicated as adjunctive therapy for the treatment of my…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68001-404

What is NDC 68001-404?: 68001-404 is the product NDC for Levetiracetam, Levetiracetam 750 mg/1 tablet, film coated, listed with the FDA by BluePoint Laboratories. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Levetiracetam.
What is the active ingredient?: Levetiracetam.
Who is the labeler?: BluePoint Laboratories, NDC labeler code 68001. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Levetiracetam?: 260 other product NDCs are listed under this name. See all Levetiracetam 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 Levetiracetam NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-0288	55154-0288-00
Levetiracetam	Levetiracetam 750 mg/1	Tablet, Film coated, Extended releaseOral	REMEDYREPACK INC.	70518-4731	70518-4731-00
Levetiracetam	Levetiracetam 100 mg/mL	Injection, Solution, ConcentrateIntravenous	Baxter Healthcare Corporation	36000-265	36000-0265-0536000-0265-10
Levetiracetam	Levetiracetam 1000 mg/1	TabletOral	Direct_Rx	72189-679	72189-0679-6072189-0679-82
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Unit Dose Solutions, Inc.	87441-046	87441-0046-01
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0420	67046-0420-03
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Injecta Medcial LLC	87234-0035	87234-0035-01
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0863	67046-0863-03
Levetiracetam	Levetiracetam 500 mg/1	TabletOral	Coupler LLC	67046-2094	67046-2094-03
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0880	67046-0880-03

All 261 Levetiracetam NDCs

Other NDCs under ANDA 078993

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

FDA NDC Directory listings under ANDA 078993
Product	Strength	Form · route	Labeler	Product NDC
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7123
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7124
Levetiracetam	Levetiracetam 750 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-7125
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7768
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7770
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7771
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7774
Levetiracetam	Levetiracetam 750 mg/1	Tablet, Film coatedOral	A-S Medication Solutions	50090-7775
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-3367
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-4171
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-657
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	American Health Packaging	60687-668
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-315
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0420
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0863
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Coupler LLC	67046-0880
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-402
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-403
Levetiracetam	Levetiracetam 1000 mg/1	Tablet, Film coatedOral	BluePoint Laboratories	68001-405
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	American Health Packaging	68084-859

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