NDC codes

FDA NDC Directory
Product NDC (as listed)0615-8623Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00615-8623Add 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
0615-8623-39006158623390061586233930 TABLET, CHEWABLE in 1 BLISTER PACK (0615-8623-39)Marketed from Feb 10, 2026

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)
Phenytoin
Generic name (nonproprietary)
phenytoin
Active ingredients
Phenytoin — 50 mg/1
Dosage form
Tablet, Chewable
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 200565
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 0615-8623_efe57937-39ce-420b-a611-68d08a7b246dSPL ID efe57937-39ce-420b-a611-68d08a7b246dSPL set ID 98bd1d9f-b1a4-49eb-a0b4-a790265710ddRxCUI 1313885UNII 6158TKW0C5
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

N400615862339 followed by a unit qualifier and the quantity

Package 00615-8623-39. 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)

Phenytoin chewable tablets are indicated for the treatment of generalized tonic-clonic (grand mal) and complex partial (psychomotor, temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery. Phenytoin chewable tablets are indicated for the treatment of generalized tonic-clonic (grand mal) and complex partial (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 0615-8623

What is NDC 0615-8623?
0615-8623 is the product NDC for Phenytoin, Phenytoin 50 mg/1 tablet, chewable, 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?
Phenytoin.
What is the active ingredient?
Phenytoin.
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 Phenytoin?
10 other product NDCs are listed under this name. See all Phenytoin 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 Phenytoin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralRising Pharma Holdings, Inc.64980-57364980-0573-01
PhenytoinPhenytoin 125 mg/5mLSuspensionOralMylan Pharmaceuticals Inc.59762-053159762-0531-02
PhenytoinPhenytoin 125 mg/5mLSuspensionOralAmerican Health Packaging60687-27560687-0275-66
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralREMEDYREPACK INC.70518-084170518-0841-0070518-0841-03
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralAmerican Health Packaging60687-15660687-0156-25
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralMajor Pharmaceuticals0904-719900904-7199-07
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralSun Pharmaceutical Industries, Inc.51672-414651672-4146-0151672-4146-0351672-4146-06
PhenytoinPhenytoin 125 mg/5mLSuspensionOralPAI Holdings, LLC dba PAI Pharma0121-089200121-0892-63
PhenytoinPhenytoin 125 mg/5mLSuspensionOralATLANTIC BIOLOGICALS CORP.17856-407017856-4070-01
PhenytoinPhenytoin 125 mg/5mLSuspensionOralSun Pharmaceutical Industries, Inc.51672-406951672-4069-02

Other NDCs under ANDA 200565

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

FDA NDC Directory listings under ANDA 200565
ProductStrengthForm · routeLabelerProduct NDC
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralMajor Pharmaceuticals0904-7199
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralSun Pharmaceutical Industries, Inc.51672-4146
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralAmerican Health Packaging60687-156
PhenytoinPhenytoin 50 mg/1Tablet, ChewableOralREMEDYREPACK INC.70518-0841

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