Dexmethylphenidate Hydrochloride NDC 72162-1473

Product information

Brand name (proprietary)

Dexmethylphenidate Hydrochloride

Generic name (nonproprietary)

dexmethylphenidate hydrochloride

Active ingredients

Dexmethylphenidate hydrochloride — 10 mg/1

Dosage form

Capsule, Extended release

Route

Oral

Labeler

Bryant Ranch Prepack

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 202842

Marketing start

Jan 5, 2017

Listing expires

Dec 31, 2026

DEA schedule

CII

Other FDA classes

Central Nervous System Stimulation (Physiologic effect)

Identifiers

Product ID 72162-1473_4a7ad9cd-cf63-4cd3-b6d3-42703d9f9e00SPL ID 4a7ad9cd-cf63-4cd3-b6d3-42703d9f9e00SPL set ID b82e8d08-cc4a-40a6-85a5-07717f3cb38bRxCUI 899439UNII 1678OK0E08

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

N472162147301 followed by a unit qualifier and the quantity Copy

Package 72162-1473-01. 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

Other NDCs under ANDA 202842

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