What is NDC 63629-4137?

63629-4137 is the product NDC for Levetiracetam, Levetiracetam 500 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 package NDCs, shown above in 10- and 11-digit form.

Bryant Ranch Prepack, NDC labeler code 63629. 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?

261 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 63629-4137 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)63629-4137Labeler and product segments. Claims need a package NDC.

Product NDC at billing width63629-4137Add 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
63629-4137-1	63629413701	90 TABLET, FILM COATED in 1 BOTTLE (63629-4137-1)Marketed from Feb 18, 2010
63629-4137-2	63629413702	60 TABLET, FILM COATED in 1 BOTTLE (63629-4137-2)Marketed from Sep 6, 2011
63629-4137-3	63629413703	30 TABLET, FILM COATED in 1 BOTTLE (63629-4137-3)Marketed from Feb 24, 2012
63629-4137-4	63629413704	120 TABLET, FILM COATED in 1 BOTTLE (63629-4137-4)Marketed from Apr 19, 2013
63629-4137-5	63629413705	28 TABLET, FILM COATED in 1 BOTTLE (63629-4137-5)Marketed from Mar 6, 2023
63629-4137-6	63629413706	100 TABLET, FILM COATED in 1 BOTTLE (63629-4137-6)Marketed from Mar 6, 2023
63629-4137-7	63629413707	21 TABLET, FILM COATED in 1 BOTTLE (63629-4137-7)Marketed from Apr 2, 2024
63629-4137-8	63629413708	180 TABLET, FILM COATED in 1 BOTTLE (63629-4137-8)Marketed from Apr 2, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Bryant Ranch PrepackNDC labeler code 63629
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078154
Marketing start: Jan 15, 2009
Listing expires: Dec 31, 2027
Other FDA classes: Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers: Product ID 63629-4137_505a2d97-ea8d-4e3a-9af7-95df7f59d89bSPL ID 505a2d97-ea8d-4e3a-9af7-95df7f59d89bSPL set ID 24f815ef-58e6-42b9-8137-adcd6c382aa6RxCUI 311289UNII 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

N463629413701 followed by a unit qualifier and the quantity

Package 63629-4137-01. 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 Apr 2, 2026.

Indications (excerpt from the label)

Levetiracetam tablets USP are indicated for the treatment of partial-onset seizures in patients 1 month of age and older (1.1) Levetiracetam tablets USP are indicated for adjunctive therapy for treatment of: Partial onset seizures in patients one month of age and older with epilepsy ( 1.1 ) 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 USP are indicated for treatment of partial-onset seizures in patients 1 month of age and older. 1.2 Myoclonic Seizures in Patients with J…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63629-4137

What is NDC 63629-4137?: 63629-4137 is the product NDC for Levetiracetam, Levetiracetam 500 mg/1 tablet, film coated, listed with the FDA by Bryant Ranch Prepack. It has 8 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?: Bryant Ranch Prepack, NDC labeler code 63629. 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?: 261 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 262 Levetiracetam NDCs

Other NDCs under ANDA 078154

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

FDA NDC Directory listings under ANDA 078154
Product	Strength	Form · route	Labeler	Product NDC
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	PD-Rx Pharmaceuticals, Inc.	43063-617
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Proficient Rx LP	63187-360
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-4675
Levetiracetam	Levetiracetam 250 mg/1	Tablet, Film coatedOral	Lupin Pharmaceuticals, Inc.	68180-112
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Lupin Pharmaceuticals, Inc.	68180-113
Levetiracetam	Levetiracetam 750 mg/1	Tablet, Film coatedOral	Lupin Pharmaceuticals, Inc.	68180-114
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals, Inc.	68788-8254
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-1108
Levetiracetam	Levetiracetam 500 mg/1	Tablet, Film coatedOral	REMEDYREPACK INC.	70518-1772
Levetiracetam	Levetiracetam 750 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	71335-2098