NDC codes

FDA NDC Directory
Product NDC (as listed)65862-692Labeler and product segments. Claims need a package NDC.
Product NDC at billing width65862-0692Add 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
65862-692-016586206920165862069201100 CAPSULE in 1 BOTTLE (65862-692-01)Marketed from Jun 10, 2015
65862-692-78658620692786586206927810 BLISTER PACK in 1 CARTON (65862-692-78) / 10 CAPSULE in 1 BLISTER PACK (65862-692-10)Marketed from Jun 10, 2015
65862-692-9965862069299658620692991000 CAPSULE in 1 BOTTLE (65862-692-99)Marketed from Jun 10, 2015

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)
Extended Phenytoin Sodium
Generic name (nonproprietary)
phenytoin sodium
Active ingredients
Phenytoin sodium — 100 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Aurobindo Pharma LimitedNDC labeler code 65862
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 204309
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 1A2 Inducers (Mechanism)Cytochrome P450 2B6 Inducers (Mechanism)Cytochrome P450 2C19 Inducers (Mechanism)Cytochrome P450 2C8 Inducers (Mechanism)Cytochrome P450 2C9 Inducers (Mechanism)Cytochrome P450 2D6 Inducers (Mechanism)Cytochrome P450 3A Inducers (Mechanism)Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 65862-692_8b54186e-7485-40f0-8fe0-58b417dfcb7eSPL ID 8b54186e-7485-40f0-8fe0-58b417dfcb7eSPL set ID 5362ea50-38a4-48b4-a85b-d634c3d8b91aRxCUI 855671UNII 4182431BJH
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

N465862069201 followed by a unit qualifier and the quantity

Package 65862-0692-01. 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)

Extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. Extended phenytoin sodium capsules are indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 65862-692

What is NDC 65862-692?
65862-692 is the product NDC for Extended Phenytoin Sodium (phenytoin sodium), Phenytoin sodium 100 mg/1 capsule, listed with the FDA by Aurobindo Pharma Limited. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Extended Phenytoin Sodium (Phenytoin Sodium).
What is the active ingredient?
Phenytoin sodium.
Who is the labeler?
Aurobindo Pharma Limited, NDC labeler code 65862. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Extended Phenytoin Sodium?
5 other product NDCs are listed under this name. See all Extended Phenytoin Sodium 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 Extended Phenytoin Sodium NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralAmerican Health Packaging60687-84160687-0841-01
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralREMEDYREPACK INC.70518-222770518-2227-03
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-855600615-8556-39
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralBryant Ranch Prepack72162-251472162-2514-0072162-2514-01
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralAmneal Pharmaceuticals LLC65162-21265162-0212-0365162-0212-1065162-0212-11+1 more

Other NDCs under ANDA 204309

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

FDA NDC Directory listings under ANDA 204309
ProductStrengthForm · routeLabelerProduct NDC
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8556
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralAmerican Health Packaging60687-841
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralREMEDYREPACK INC.70518-2227
Extended Phenytoin Sodiumphenytoin sodiumPhenytoin sodium 100 mg/1CapsuleOralBryant Ranch Prepack72162-2514

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