Dexmethylphenidate — ingredient monograph

Overview

Source: NDC Directory

Ingredient name

DEXMETHYLPHENIDATE HYDROCHLORIDE

Base moiety

DEXMETHYLPHENIDATE

RxNorm CUI

899439

UNII

1678OK0E08

Medication products

11

Brand names

4

Dosage forms

4

FAERS reports

58,466 · not a risk measure

Products containing this ingredient

Source: NDC Directory 11 products

d-Methylphenidate Hydrochloride Powder
1 NDC
dex-Methylphenidate Hydrochloride Powder
1 NDC
Dexmethylphenidate HCl Powder
1 NDC
Dexmethylphenidate Hydrochloride Powder
6 NDC
Dexmethylphenidate Hydrochloride Capsule
7 NDC
Methylphenidate Hydrochloride Capsule
2 NDC
AZSTARYS Serdexmethylphenidate and Dexmethylphenidate · Capsule
Rx NDA 3 NDC
dexmethylphenidate hydrochloride Capsule, Extended Release
Rx ANDA TE AB 86 NDC
dexmethylphenidate hydrochloride Tablet
Rx ANDA TE AB 25 NDC
Focalin dexmethylphenidate hydrochloride · Capsule, Extended Release
Rx NDA TE AB 1 recall 16 NDC
Focalin dexmethylphenidate hydrochloride · Tablet
Rx NDA TE AB 3 NDC

Entries without a link are products listed by the FDA that carry no approval record, therapeutic equivalence rating or official labelling, so they have no detail page. Their facts are shown inline.

By dosage form

How this ingredient is presented across the catalogue.
Dosage form	Products	Examples
Powder	4	d-Methylphenidate Hydrochloride, dex-Methylphenidate Hydrochloride, Dexmethylphenidate HCl, Dexmethylphenidate Hydrochloride
Capsule	3	Dexmethylphenidate Hydrochloride, Methylphenidate Hydrochloride, AZSTARYS
CAPSULE, Extended Release	2	dexmethylphenidate hydrochloride, Focalin
Tablet	2	dexmethylphenidate hydrochloride, Focalin

Sources for this page

Dataset	Agency	Used for
NDC Directory	FDA	Ingredient name, strengths, products, labelers, packages
DailyMed RxNorm mappings	NLM	RxNorm concept identifier (RxCUI)
FAERS	FDA	Adverse event report totals