NDC 10702-106 – Dexmethylphenidate Hydrochloride

Dexmethylphenidate Hydrochloride 2.5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC10702-106

Product details

Brand name
Dexmethylphenidate Hydrochloride
Generic name
Dexmethylphenidate Hydrochloride
Labeler
KVK-TECH, INC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206931
Marketed since
December 4, 2015
Listing expires
December 31, 2026
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

Uses, dosage, side effects and warnings for Dexmethylphenidate Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
10702-106-01100 TABLET in 1 BOTTLE (10702-106-01)Dec 4, 2015

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