NDC codes

FDA NDC Directory
Product NDC (as listed)82804-952Labeler and product segments. Claims need a package NDC.
Product NDC at billing width82804-0952Add 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
82804-952-008280409520082804095200100 TABLET in 1 BOTTLE, PLASTIC (82804-952-00)Marketed from Jan 12, 2026
82804-952-1182804095211828040952111000 TABLET in 1 BOTTLE, PLASTIC (82804-952-11)Marketed from Jan 12, 2026
82804-952-30828040952308280409523030 TABLET in 1 BOTTLE, PLASTIC (82804-952-30)Marketed from Jan 12, 2026
82804-952-558280409525582804095255500 TABLET in 1 BOTTLE, PLASTIC (82804-952-55)Marketed from Jan 12, 2026
82804-952-60828040952608280409526060 TABLET in 1 BOTTLE, PLASTIC (82804-952-60)Marketed from Jan 12, 2026
82804-952-728280409527282804095272120 TABLET in 1 BOTTLE, PLASTIC (82804-952-72)Marketed from Jan 12, 2026
82804-952-90828040952908280409529090 TABLET in 1 BOTTLE, PLASTIC (82804-952-90)Marketed from Jan 12, 2026

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)
Primidone
Generic name (nonproprietary)
primidone
Active ingredients
Primidone — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 82804
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040586
Marketing start
Listing expires
Other FDA classes
Decreased Central Nervous System Disorganized Electrical Activity (Physiologic effect)
Identifiers
Product ID 82804-952_db761e34-8573-4f96-872c-e851b3004e5eSPL ID db761e34-8573-4f96-872c-e851b3004e5eSPL set ID db761e34-8573-4f96-872c-e851b3004e5eRxCUI 96304, 198150UNII 13AFD7670QUPC 0382804953301, 0382804952304
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

N482804095200 followed by a unit qualifier and the quantity

Package 82804-0952-00. 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)

INDICATIONS AND USAGE Primidone, used alone or concomitantly with other anticonvulsants, is indicated in the control of grand mal, psychomotor, and focal epileptic seizures. It may control grand mal seizures refractory to other anticonvulsant therapy.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 82804-952

What is NDC 82804-952?
82804-952 is the product NDC for Primidone, Primidone 50 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 7 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Primidone.
What is the active ingredient?
Primidone.
Who is the labeler?
Proficient Rx LP, NDC labeler code 82804. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Primidone?
41 other product NDCs are listed under this name. See all Primidone 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 Primidone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PrimidonePrimidone 50 mg/1TabletOralNorthStar Rx LLC72603-60972603-0609-0172603-0609-02
PrimidonePrimidone 250 mg/1TabletOralNorthStar Rx LLC72603-61072603-0610-01
PrimidonePrimidone 50 mg/1TabletOralCarnegie Pharmaceuticals LLC80005-11780005-0117-1180005-0117-1480005-0117-15
PrimidonePrimidone 250 mg/1TabletOralCarnegie Pharmaceuticals LLC80005-11880005-0118-1180005-0118-1480005-0118-15
PrimidonePrimidone 50 mg/1TabletOralAdvagen Pharma Limited72888-04572888-0045-0172888-0045-05
PrimidonePrimidone 250 mg/1TabletOralAdvagen Pharma Limited72888-04672888-0046-0172888-0046-05
PrimidonePrimidone 125 mg/1TabletOralAdvagen Pharma Limited72888-16072888-0160-0072888-0160-0172888-0160-05+1 more
PrimidonePrimidone 125 mg/1TabletOralTruPharma LLC.52817-11752817-0117-1052817-0117-3052817-0117-50
PrimidonePrimidone 50 mg/1TabletOralAvKARE42291-50942291-0509-50
PrimidonePrimidone 250 mg/1TabletOralAvKARE42291-51142291-0511-01

All 42 Primidone NDCs

Other NDCs under ANDA 040586

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

FDA NDC Directory listings under ANDA 040586
ProductStrengthForm · routeLabelerProduct NDC
PrimidonePrimidone 50 mg/1TabletOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8664
PrimidonePrimidone 50 mg/1TabletOralOxford Pharmaceuticals, LLC69584-684
PrimidonePrimidone 250 mg/1TabletOralOxford Pharmaceuticals, LLC69584-685
PrimidonePrimidone 50 mg/1TabletOralBryant Ranch Prepack71335-1965
PrimidonePrimidone 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-540
PrimidonePrimidone 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-590
PrimidonePrimidone 50 mg/1TabletOralDIRECT RX72189-216
PrimidonePrimidone 250 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-177
PrimidonePrimidone 50 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-178
PrimidonePrimidone 250 mg/1TabletOralProficient Rx LP82804-953

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