NDC codes

FDA NDC Directory
Product NDC (as listed)13668-539Labeler and product segments. Claims need a package NDC.
Product NDC at billing width13668-0539Add 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
13668-539-0513668053905500 TABLET in 1 BOTTLE (13668-539-05)Marketed from May 6, 2025
13668-539-301366805393030 TABLET in 1 BOTTLE (13668-539-30)Marketed from May 6, 2025
13668-539-601366805396060 TABLET in 1 BOTTLE (13668-539-60)Marketed from May 6, 2025

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)
Eslicarbazepine acetate
Generic name (nonproprietary)
eslicarbazepine acetate
Active ingredients
Eslicarbazepine acetate — 400 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Torrent Pharmaceuticals LimitedNDC labeler code 13668
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211227
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 2C19 Inhibitors (Mechanism)Cytochrome P450 3A4 Inducers (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 13668-539_3b2943e4-21ea-828b-e063-6294a90a275bSPL ID 3b2943e4-21ea-828b-e063-6294a90a275bSPL set ID d279e461-2611-4f5c-938d-5d117612894fRxCUI 1482507, 1482515, 1482521, 1482525UNII BEA68ZVB2KUPC 0313668540307, 0313668539301, 0313668538304, 0313668541304

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

N413668053905 followed by a unit qualifier and the quantity

Package 13668-0539-05. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Eslicarbazepine acetate tablets are indicated for the treatment of partial-onset seizures in patients 4 years of age and older. Eslicarbazepine acetate tablets are indicated for the treatment of partial-onset seizures in patients 4 years of age and older.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 13668-539

What is NDC 13668-539?
13668-539 is the product NDC for Eslicarbazepine acetate, Eslicarbazepine acetate 400 mg/1 tablet, listed with the FDA by Torrent Pharmaceuticals Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Eslicarbazepine acetate.
What is the active ingredient?
Eslicarbazepine acetate.
Who is the labeler?
Torrent Pharmaceuticals Limited, NDC labeler code 13668. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eslicarbazepine acetate?
35 other product NDCs are listed under this name. See all Eslicarbazepine acetate 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 Eslicarbazepine acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Eslicarbazepine AcetateEslicarbazepine acetate 200 mg/1TabletOralAurobindo Pharma Limited59651-53359651-0533-30
Eslicarbazepine AcetateEslicarbazepine acetate 400 mg/1TabletOralAurobindo Pharma Limited59651-53459651-0534-30
Eslicarbazepine AcetateEslicarbazepine acetate 600 mg/1TabletOralAurobindo Pharma Limited59651-53559651-0535-60
Eslicarbazepine AcetateEslicarbazepine acetate 800 mg/1TabletOralAurobindo Pharma Limited59651-53659651-0536-30
Eslicarbazepine AcetateEslicarbazepine acetate 200 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-71759746-0717-1059746-0717-3059746-0717-90
Eslicarbazepine AcetateEslicarbazepine acetate 400 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-71859746-0718-1059746-0718-3059746-0718-90
Eslicarbazepine AcetateEslicarbazepine acetate 600 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-71959746-0719-0559746-0719-3059746-0719-60+1 more
Eslicarbazepine AcetateEslicarbazepine acetate 800 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-72059746-0720-0559746-0720-3059746-0720-90
Eslicarbazepine acetateEslicarbazepine acetate 200 mg/1TabletOralTorrent Pharmaceuticals Limited13668-53813668-0538-0513668-0538-3013668-0538-60
Eslicarbazepine acetateEslicarbazepine acetate 600 mg/1TabletOralTorrent Pharmaceuticals Limited13668-54013668-0540-0513668-0540-3013668-0540-60

All 36 Eslicarbazepine acetate NDCs

Other NDCs under ANDA 211227

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

FDA NDC Directory listings under ANDA 211227
ProductStrengthForm · routeLabelerProduct NDC
Eslicarbazepine acetateEslicarbazepine acetate 200 mg/1TabletOralTorrent Pharmaceuticals Limited13668-538
Eslicarbazepine acetateEslicarbazepine acetate 600 mg/1TabletOralTorrent Pharmaceuticals Limited13668-540
Eslicarbazepine acetateEslicarbazepine acetate 800 mg/1TabletOralTorrent Pharmaceuticals Limited13668-541

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