NDC 10702-101 – Methylphenidate Hydrochloride

Methylphenidate Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC10702-101

Product details

Brand name
Methylphenidate Hydrochloride
Generic name
Methylphenidate Hydrochloride
Labeler
KVK-TECH, INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA206932
Marketed since
May 11, 2017
Listing expires
December 31, 2027
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
10702-101-01100 TABLET in 1 BOTTLE (10702-101-01)May 11, 2017

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