NDC codes

FDA NDC Directory
Product NDC (as listed)70377-117Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70377-0117Add 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
70377-117-1170377011711703770117111 BOTTLE in 1 CARTON (70377-117-11) / 250 mL in 1 BOTTLEMarketed from May 31, 2024

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)
Oxcarbazepine
Generic name (nonproprietary)
oxcarbazepine
Active ingredients
Oxcarbazepine — 60 mg/mL
Dosage form
Suspension
Route
Oral
Labeler
Biocon Pharma Inc.NDC labeler code 70377
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218278
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 70377-117_3a03d0df-81f9-c49e-c812-a713524a7de0SPL ID 3a03d0df-81f9-c49e-c812-a713524a7de0
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

N470377011711 followed by a unit qualifier and the quantity

Package 70377-0117-11. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70377-117

What is NDC 70377-117?
70377-117 is the product NDC for Oxcarbazepine, Oxcarbazepine 60 mg/mL suspension, listed with the FDA by Biocon Pharma Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxcarbazepine.
What is the active ingredient?
Oxcarbazepine.
Who is the labeler?
Biocon Pharma Inc., NDC labeler code 70377. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxcarbazepine?
118 other product NDCs are listed under this name. See all Oxcarbazepine 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 Oxcarbazepine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralZameer Pharmaceuticals LLC90096-17190096-0171-01
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralZameer Pharmaceuticals LLC90096-17290096-0172-01
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralZameer Pharmaceuticals LLC90096-17390096-0173-01
OxcarbazepineOxcarbazepine 300 mg/5mLSuspensionOralNovadoz Pharmaceuticals LLC72205-35472205-0354-85
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-466470518-4664-0070518-4664-01
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralREMEDYREPACK INC.70518-466370518-4663-0070518-4663-01
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralCoupler LLC67046-208467046-2084-03
OxcarbazepineOxcarbazepine 300 mg/1Tablet, Film coatedOralCoupler LLC67046-086867046-0868-03
OxcarbazepineOxcarbazepine 600 mg/1Tablet, Film coatedOralCoupler LLC67046-017967046-0179-03
OxcarbazepineOxcarbazepine 150 mg/1Tablet, Film coatedOralMajor Pharmaceuticals0904-759300904-7593-61

All 119 Oxcarbazepine NDCs

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