NDC codes

FDA NDC Directory
Product NDC (as listed)59746-717Labeler and product segments. Claims need a package NDC.
Product NDC at billing width59746-0717Add 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
59746-717-10597460717101000 TABLET in 1 BOTTLE (59746-717-10)Marketed from May 1, 2026
59746-717-305974607173030 TABLET in 1 BOTTLE (59746-717-30)Marketed from May 1, 2026
59746-717-905974607179090 TABLET in 1 BOTTLE (59746-717-90)Marketed from May 1, 2026

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 — 200 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Jubilant Cadista Pharmaceuticals Inc.NDC labeler code 59746
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 211219
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 59746-717_196ec23c-8453-4396-b6c4-d6934a418787SPL ID 196ec23c-8453-4396-b6c4-d6934a418787SPL set ID 22d08671-ac0d-4e3d-8195-929bbb021125RxCUI 1482507, 1482515, 1482521, 1482525UNII BEA68ZVB2KUPC 0359746717308

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

N459746071710 followed by a unit qualifier and the quantity

Package 59746-0717-10. 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. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 59746-717

What is NDC 59746-717?
59746-717 is the product NDC for Eslicarbazepine Acetate, Eslicarbazepine acetate 200 mg/1 tablet, listed with the FDA by Jubilant Cadista Pharmaceuticals Inc.. 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?
Jubilant Cadista Pharmaceuticals Inc., NDC labeler code 59746. 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 600 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-71959746-0719-0559746-0719-3059746-0719-60+1 more
Eslicarbazepine AcetateEslicarbazepine acetate 400 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-71859746-0718-1059746-0718-3059746-0718-90
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 400 mg/1TabletOralTorrent Pharmaceuticals Limited13668-53913668-0539-0513668-0539-3013668-0539-60
Eslicarbazepine acetateEslicarbazepine acetate 600 mg/1TabletOralTorrent Pharmaceuticals Limited13668-54013668-0540-0513668-0540-3013668-0540-60

All 36 Eslicarbazepine Acetate NDCs

Other NDCs under ANDA 211219

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

FDA NDC Directory listings under ANDA 211219
ProductStrengthForm · routeLabelerProduct NDC
Eslicarbazepine AcetateEslicarbazepine acetate 600 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-719
Eslicarbazepine AcetateEslicarbazepine acetate 400 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-718
Eslicarbazepine AcetateEslicarbazepine acetate 800 mg/1TabletOralJubilant Cadista Pharmaceuticals Inc.59746-720

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