NDC codes

FDA NDC Directory
Product NDC (as listed)70518-3940Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70518-3940Add 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
70518-3940-07051839400030 TABLET, FILM COATED in 1 BLISTER PACK (70518-3940-0)Marketed from Dec 6, 2023
70518-3940-170518394001100 POUCH in 1 BOX (70518-3940-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2)Marketed from Feb 24, 2024

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)
Oxcarbazepine
Generic name (nonproprietary)
oxcarbazepine
Active ingredients
Oxcarbazepine150 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215939
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 70518-3940_53fa4ffb-bfe6-663a-e063-6394a90a884aSPL ID 53fa4ffb-bfe6-663a-e063-6394a90a884aSPL set ID 188a48ad-c412-416a-b15b-de5f232740a2RxCUI 312136UNII VZI5B1W380
Pharmacologic class
Anti-epileptic Agent

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

N470518394000 followed by a unit qualifier and the quantity

Package 70518-3940-00. 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)

Oxcarbazepine tablets are indicated for use as monotherapy or adjunctive therapy in the treatment of partial-onset seizures in adults and as monotherapy in the treatment of partial-onset seizures in pediatric patients aged 4 years and above, and as adjunctive therapy in pediatric patients aged 2 years and above with partial-onset seizures. Oxcarbazepine tablets are indicated for: • Adults: Monotherapy or adjunctive therapy in the treatment of partial-onset seizures • Pediatrics: - Monotherapy in the treatment of partial-onset seizures in children 4 to 16 years - Adjunctive therapy in the treatment of partial-onset seizures in children 2 to 16 years ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 215939

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

FDA NDC Directory listings under ANDA 215939
ProductStrengthForm · routeLabelerProduct NDC
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralCoupler LLC67046-2084
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-271
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralNorthStar RxLLC72603-272
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3921
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-3925
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralProficient Rx LP82804-209
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralAvPAK50268-679
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralAvPAK50268-680
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralAvPAK50268-681
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-711
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-722
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2139
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-2138
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralAmerican Health Packaging60687-733
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-2548
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralASCLEMED USA INC.87063-208
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-023
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-024
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralCamber Pharmaceuticals, Inc.31722-025
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralXLCare Pharmaceuticals Inc.72865-284

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