NDC 0406-0136 – Methylphenidate Hydrochloride Extended-Release

Methylphenidate Hydrochloride 36 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug DEA schedule CII

Product NDC0406-0136

Product details

Brand name
Methylphenidate Hydrochloride Extended-Release
Generic name
Methylphenidate Hydrochloride
Labeler
SpecGx LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA202608
Marketed since
December 28, 2012
Marketing end
January 31, 2028
Pharmacologic class
Central Nervous System Stimulant

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0406-0136-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0406-0136-01)Dec 28, 2012

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