Prescription drug · ANDA
Extended Phenytoin Sodium (Phenytoin sodium) NDC 0615-8556
Phenytoin sodium 100 mg/1 · Capsule · Oral · NCS HealthCare of KY, LLC dba Vangard Labs
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 0615-8556-39 | 0061585563900615855639 | 30 CAPSULE in 1 BLISTER PACK (0615-8556-39)Marketed from Oct 16, 2024 |
How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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
- NCS HealthCare of KY, LLC dba Vangard LabsNDC labeler code 0615
- 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 0615-8556_8240390a-9bc8-4256-8f2a-107c97c0400cSPL ID 8240390a-9bc8-4256-8f2a-107c97c0400cSPL set ID a7bfb3aa-5226-4a48-8156-a9ecc4536fdfRxCUI 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
N400615855639followed by a unit qualifier and the quantityPackage 00615-8556-39. 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.
About NDC 0615-8556
- What is NDC 0615-8556?
- 0615-8556 is the product NDC for Extended Phenytoin Sodium (phenytoin sodium), Phenytoin sodium 100 mg/1 capsule, listed with the FDA by NCS HealthCare of KY, LLC dba Vangard Labs. It has 1 package NDC, 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?
- NCS HealthCare of KY, LLC dba Vangard Labs, NDC labeler code 0615. 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.
Related NDCs: other Extended Phenytoin Sodium products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | American Health Packaging | 60687-841 | 60687-0841-01 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-2227 | 70518-2227-03 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-692 | 65862-0692-0165862-0692-7865862-0692-99 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | Bryant Ranch Prepack | 72162-2514 | 72162-2514-0072162-2514-01 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | Amneal Pharmaceuticals LLC | 65162-212 | 65162-0212-0365162-0212-1065162-0212-11+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.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | American Health Packaging | 60687-841 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | Aurobindo Pharma Limited | 65862-692 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | REMEDYREPACK INC. | 70518-2227 |
| Extended Phenytoin Sodiumphenytoin sodium | Phenytoin sodium 100 mg/1 | CapsuleOral | Bryant Ranch Prepack | 72162-2514 |