Dexmethylphenidate Hydrochloride NDC 10702-106

NDC codes

FDA NDC Directory

Product NDC (as listed)10702-106Labeler and product segments. Claims need a package NDC.

Product NDC at billing width10702-0106Add 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 NDC	11-digit (billing)	Package	Copy
10702-106-01	10702010601	100 TABLET in 1 BOTTLE (10702-106-01)Marketed from Dec 4, 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): Dexmethylphenidate Hydrochloride
Generic name (nonproprietary): dexmethylphenidate hydrochloride
Active ingredients: Dexmethylphenidate hydrochloride — 2.5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: KVK-TECH, INC
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 206931
Marketing start: Dec 4, 2015
Listing expires: Dec 31, 2026
DEA schedule: CII
Other FDA classes: Central Nervous System Stimulation (Physiologic effect)
Identifiers: Product ID 10702-106_445dff50-b3a4-8602-e063-6294a90aef3bSPL ID 445dff50-b3a4-8602-e063-6294a90aef3bSPL set ID 0c717ae4-ec27-47db-ac1b-e504dbb379beRxCUI 899518, 899548, 899557UNII 1678OK0E08UPC 0310702108011, 0310702106017, 0310702107014
Pharmacologic class: Central Nervous System Stimulant

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

N410702010601 followed by a unit qualifier and the quantity

Package 10702-0106-01. 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 Nov 24, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Dexmethylphenidate hydrochloride tablets is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) [see Clinical Studies (14)]. Dexmethylphenidate hydrochloride tablets is a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) (1).

Excerpt only. Read the full label for complete information.

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