NDC codes

FDA NDC Directory
Product NDC (as listed)43063-499Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43063-0499Add 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 NDC11-digit (billing)PackageCopy
43063-499-604306304996060 TABLET in 1 BOTTLE, PLASTIC (43063-499-60)Marketed from Feb 9, 2012

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 — 500 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078858
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 43063-499_2f364228-05e4-2e79-e063-6294a90ac493SPL ID 2f364228-05e4-2e79-e063-6294a90ac493SPL set ID c2177034-e164-453c-be02-1cf91ce27a07RxCUI 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

N443063049960 followed by a unit qualifier and the quantity

Package 43063-0499-60. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 078858

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

FDA NDC Directory listings under ANDA 078858
ProductStrengthForm · routeLabelerProduct NDC
LevetiracetamLevetiracetam 750 mg/1TabletOralOWP Pharmaceuticals, Inc.69102-106
LevetiracetamLevetiracetam 500 mg/1TabletOralOWP Pharmaceuticals, Inc.69102-105
LevetiracetamLevetiracetam 500 mg/1TabletOralTorrent Pharmaceuticals Limited13668-015
LevetiracetamLevetiracetam 1000 mg/1TabletOralOWP Pharmaceuticals, Inc.69102-107
LevetiracetamLevetiracetam 250 mg/1TabletOralTorrent Pharmaceuticals Limited13668-014
RoweepralevetiracetamLevetiracetam 250 mg/1TabletOralOWP Pharmaceuticals, Inc.69102-108
LevetiracetamLevetiracetam 750 mg/1TabletOralTorrent Pharmaceuticals Limited13668-016
LevetiracetamLevetiracetam 1000 mg/1TabletOralTorrent Pharmaceuticals Limited13668-017
LevetiracetamLevetiracetam 500 mg/1TabletOralBryant Ranch Prepack71335-2282

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