NDC codes

FDA NDC Directory
Product NDC (as listed)68025-084Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68025-0084Add 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
68025-084-30680250084306802500843030 TABLET, EXTENDED RELEASE in 1 BOTTLE (68025-084-30)Marketed from Jun 23, 2022

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)
Relexxii
Generic name (nonproprietary)
methylphenidate hydrochloride
Active ingredients
Methylphenidate hydrochloride — 72 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Labeler
Vertical Pharmaceuticals, LLCNDC labeler code 68025
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 216117
Marketing start
Listing expires
DEA schedule
CII
Other FDA classes
Central Nervous System Stimulation (Physiologic effect)
Identifiers
Product ID 68025-084_86f477e9-07fc-466b-913e-1a4434c91df4SPL ID 86f477e9-07fc-466b-913e-1a4434c91df4SPL set ID 22d5fa47-b5b9-4fd9-980c-4eb88e95ae5dRxCUI 1091155, 1091170, 1091185, 1091210, 1995461, 2052826, 2605796, 2605798, 2605943, 2605946, 2668496, 2668499, 2668502, 2668505UNII 4B3SC438HIUPC 0368025097109, 0368025096300, 0368025096102, 0368025084307, 0368025095303, 0368025098304, 0368025095105, 0368025098106, 0368025089302, 0368025088305, 0368025097307

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

N468025008430 followed by a unit qualifier and the quantity

Package 68025-0084-30. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

RELEXXII is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults (up to the age of 65 years) and pediatric patients 6 years of age and older [ see Clinical Studies ( 14 )] . Limitations of Use The use of RELEXXII is not recommended in pediatric patients younger than 6 years of age because they had higher plasma exposure and a higher incidence of adverse reactions (e.g., weight loss) than patients 6 years and older at the same dosage [see Warnings and Precautions ( 5.7 ), Use in Specific Populations ( 8.4 )] . RELEXXII ® is a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults (up t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68025-084

What is NDC 68025-084?
68025-084 is the product NDC for Relexxii (methylphenidate hydrochloride), Methylphenidate hydrochloride 72 mg/1 tablet, extended release, listed with the FDA by Vertical Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Relexxii (Methylphenidate hydrochloride).
What is the active ingredient?
Methylphenidate hydrochloride.
Who is the labeler?
Vertical Pharmaceuticals, LLC, NDC labeler code 68025. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Relexxii?
6 other product NDCs are listed under this name. See all Relexxii 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 Relexxii NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 45 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-08868025-0088-30
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 63 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-08968025-0089-30
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 18 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-09568025-0095-1068025-0095-30
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 27 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-09668025-0096-1068025-0096-30
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 36 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-09768025-0097-1068025-0097-30
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 54 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-09868025-0098-1068025-0098-30

Other NDCs under NDA 216117

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

FDA NDC Directory listings under NDA 216117
ProductStrengthForm · routeLabelerProduct NDC
Methylphenidate HydrochlorideMethylphenidate hydrochloride 63 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-700
Methylphenidate HydrochlorideMethylphenidate hydrochloride 45 mg/1Tablet, Extended releaseOralTrigen Laboratories, LLC13811-711
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 45 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-088
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 63 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-089
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 18 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-095
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 27 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-096
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 36 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-097
Relexxiimethylphenidate hydrochlorideMethylphenidate hydrochloride 54 mg/1Tablet, Extended releaseOralVertical Pharmaceuticals, LLC68025-098

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